- Open Access
Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci
© Eggermann et al. 2015
- Received: 14 July 2015
- Accepted: 29 September 2015
- Published: 14 November 2015
The Erratum to this article has been published in Clinical Epigenetics 2016 8:27
Congenital imprinting disorders (IDs) are characterised by molecular changes affecting imprinted chromosomal regions and genes, i.e. genes that are expressed in a parent-of-origin specific manner. Recent years have seen a great expansion in the range of alterations in regulation, dosage or DNA sequence shown to disturb imprinted gene expression, and the correspondingly broad range of resultant clinical syndromes. At the same time, however, it has become clear that this diversity of IDs has common underlying principles, not only in shared molecular mechanisms, but also in interrelated clinical impacts upon growth, development and metabolism. Thus, detailed and systematic analysis of IDs can not only identify unifying principles of molecular epigenetics in health and disease, but also support personalisation of diagnosis and management for individual patients and families.
- Imprinting disorders
- Imprinted genes
- Uniparental disomy
Imprinting disorders (IDs) are a group of congenital diseases characterised by overlapping clinical features affecting growth, development and metabolism, and common molecular disturbances, affecting genomically imprinted chromosomal regions and genes. The term genomic imprinting describes the expression of specific genes in a parent-of-origin specific manner - i.e. they are expressed only from the maternal or from the paternal gene copy, but not biparentally. Disturbances of imprinted genes may alter their regulation (“epigenetic mutation") and dosage and rarely their genomic sequences can be altered (“genetic mutation”).
So far, more than 150 human genes have been shown to be imprinted (for review, http://www.geneimprint.com/site/genes-by-species), but it is likely that more remain to be identified. Imprinting marks, like other epigenetic marks, are re-established at each generation by successive removal and re-establishment in the germ cell lineages, and then in early zygotic development. The critical difference between imprinting marks and all others is that they elude postzygotic reprogramming, and therefore are essentially ubiquitous and permanent in somatic tissues - except for the germline lineage that embarks upon the establishment of the subsequent generation (for review, ).
In IDs, the regulation of imprinted genes and imprinting clusters are disturbed by different changes. In the majority of ID patients only the disease-specific loci are affected, but an increasing number of individuals have been shown to have disturbed methylation at multiple imprinted loci, the so-called multilocus methylation imprinting disturbances (MLID). Another extreme example of unbalanced imprinting patterns is uniparental diploidy (e.g. complete hydatidiform moles, where all the chromosomes are of paternal origin) or triploidies (e.g. partial hydatidiform moles where an extra haploid set of chromosomes of either maternal or paternal origin is present). These cases are not viable. However, mosaic genomewide uniparental isodiploidy has been reported to be compatible with life (for review, ).
Overview on the molecular findings in the currently known IDs and their clinical characteristics
Type of mutation/epimutation and their frequencies
Main clinical features
Transient Neonatal Diabetes Mellitus (TNDM)
6q24: PLAGL1: alt-TSS
IUGR, transient diabetes, hyperglycemia without ketoacidosis, macroglossia, omphalocele
Up to 50 %
Chromosome 6, 6q16.1qter
Silver-Russell syndrome (SRS; Russell-Silver Syndrome, RSS)
IUGR/PNGR, small prematurely calcified placenta, rel. macrocephaly at birth, hemihypotrophy, prominent forehead, triangular face, feeding difficulties
Genome-wide uniparental diploidy
Up to 50 %
H19/IGF2: IG DMR
1 family reported
In familial cases: up to 50 % in case of maternal transmission
1 family reported
Beckwith-Wiedemann syndrome (BWS; Wiedemann-Beckwith syndrome, EMG)
Pre- and postnatal overgrowth, organomegaly, macroglossia, omphalocele, neonatal hypoglycemia, hemihypertrophy, increased tumour risk
Genome-wide uniparental diploidy
Up to 50 %
IH19/IGF2: IG DMR; KCNQ1OT1: TSS-DMR
5 % (sporadic) 40–50 % (families)
Up to 50 %
Kagami-Ogata syndrome (KOS14; upd(14)pat syndrome)
in case of RT
IUGR, polyhydramnion, abdominal and thoracal wall defects, bell-shaped thorax, coat-hanger ribs
MEG3/DLK1: IG DMR
up to 50 %
MEG3: TSS DMR
Temple syndrome (TS14; upd(14)mat syndrome)
In case of RT
IUGR/PNGR, neonatal hypotonia, feeding difficulties in infancy, truncal obesity, scoliosis, precocious puberty, small feed and hands
MEG3/DLK1: IG DMR
Up to 50 %
MEG3: TSS DMR
Prader-Willi syndrome (PWS)
Up to 50 %
PNGR, mental retardation, neonatal hypotonia, hypogenitalism, hypopigmentation, obesity/hyperphagia
In case of RT
Angelman syndrome (AS)
Up to 50 %
mental retardation, microcephaly, no speech, unmotivated laughing, ataxia, seizures, scoliosis
In case of RT
In familial cases: up to 50 % in case of maternal transmission
Precocious puberty (central precocious puberty 2; cppb2)
In familial cases: up to 50 % in case of paternal transmission
Early activation of the hypothalamic-pituitary-gonadal axis results in gonadotropin-dependent precocious puberty
upd(16)mat, often associated with chromosomal aberrations
IUGR (40-85 %); heterogeneous, but no specific or unique symptoms
Pseudohypo-parathyroidism (PHP1B, PHP1C, PHP1A)
Maternally inherited deletions causing aberrant methylation
Up to 50 % in case of maternal transmission
Resistance to PTH and other hormones; Albright hereditary osteodystrophy, subcutaneous ossifications, feeding behaviour anomalies, abnormal growth patterns
maternal and paternal heterozygous loss of function mutations in GNAS coding sequence
Up to 50 % in case of maternal transmission
IUGR, PNGR, feeding difficulties
Since the genetic counseling for each ID is affected by both its familial inheritance and its underlying pathogenetic mechanism, precise molecular diagnosis is essential for accurate management and reproductive counseling. Furthermore, in some IDs somatic and germline mosaicism have been reported, a finding which may be difficult to diagnose, but must be considered since it may compromise molecular genetic testing.
Uniparental Disomy (UPD)
UPD is the inheritance of both chromosomal homologues from the same parent and has been reported for nearly all IDs (Table 1; for review, ). The recurrence risk for another child with UPD is generally low with the exception of those UPDs affecting acrocentric chromosomes (chromosomes 14 and 15): these chromosomes are prone to Robertsonian translocations (RT) which predispose to non-disjunctional errors and thus a UPD formation. However, the risk to have a child with UPD is below 1 %, but prenatal testing for UPD is recommended in carriers of balanced translocations affecting chromosomes carrying imprinted genes .
Chromosomal rearrangements (deletions, duplications, translocations)
Chromosomal imbalances either cause a loss of a gene and thereby a loss of expression of an imprinted gene in case of deletions or translocations or they result in an overexpression by duplication of imprinted chromosomal material. However, due to the complex regulation mechanisms in imprinted regions, loss of chromosomal material can also indirectly cause an overexpression of an imprinted gene due to the removal of a negative cis-acting element and vice versa (e.g. [5–7]).
In some IDs, deletions account for the majority of cases, e.g. in Angelman syndrome (AS) and Prader-Willi syndrome (PWS). They can either occur de novo, or they can be caused by inherited chromosomal rearrangements (e.g. RT). In case of familial cases, the parent-of-origin-dependent gene expression results in autosomal-dominant inheritance with a parent-of-origin-dependant penetrance.
Intragenic mutations in imprinted genes
So far, genomic point mutations in imprinted genes have only been reported for Beckwith-Wiedemann syndrome (BWS), Silver-Russell syndrome (SRS), AS, precocious puberty and pseudohypoparathyoridism (PHP) (Table 1). In precocious puberty syndrome (central precocious puberty 2; cppb2), MKRN3 mutations are the only causative molecular alterations known so far. In the other IDs, their significance differs: AS mutations in the UBE3A contribute to 10–15 % of cases, and approximately 30 % are inherited. In PHP, mutations on the coding maternal allele of GNAS are responsible for 70 % of type 1A disease (~50 % of total PHP), whereas, deletions of genomic regulatory regions have been identified in 20–30 % of the 1B subtype (~8.5 % of total PHP) . In BWS, inhibiting CDKN1C mutations can be detected, in SRS, only one case with an activating CDKN1C mutation has been reported so far . To further determine the recurrence risk in the families of these patients, familial segregation studies should be offered to establish the maternal/paternal inheritance or lack thereof, even when parents do not show obvious clinical features.
Epimutations aberrant methylation of a differentially methylated region (DMR) without alteration of the same genomic DNA sequence account for up to 50 % of molecular changes in IDs (Table 1). To contribute to the full clinical picture of an ID, hypo- or hypermethylation should affect the disease-specific germ-line DMR (e.g. the H19-DMR in 11p15), but in several IDs the methylation at further DMRs (e.g. IGF2-DMRs in 11p15) is altered  and might influence the severity of an ID (e.g. Kagami-Ogata syndrome/KOS14, ). Epimutation can occur as a result of a DNA mutation in a cis- or trans-acting factor (“secondary epimutation”), or as a primary epimutation in the absence of any DNA sequence change (“primary epimutation”). Primary epimutations often occur after fertilization and lead to somatic mosaicism. It has been estimated that the rate of primary epimutations is 1 or 2 orders of magnitude greater than somatic DNA mutations  and is associated with assisted reproductive technology , in keeping with environmental disturbances.
In terms of molecular mechanism, the four causes of IDs can interact: chromosomal translocations can predispose to both imbalances and UPD, and deletions or point mutations in regulatory domains can affect the imprinting status of a DMR [6, 10, 14]. It is noteworthy that some molecular changes may occur postzygotically, resulting in a mosaic distribution. Mosaicism can obscure genotype-phenotype correlation and is also associated with somatic asymmetry; and discordant monozygotic twinning, which can be regarded as an extreme expression of epigenetic asymmetry, is a common feature in IDs (for review, ). It may also render difficult the molecular diagnosis if the analysed tissue is not or poorly epigenetically modified.
Comparison of the major clinical findings in the known and suggested IDs, showing a broad clinical overlap between the different disorders
number of patients
ID specific chromosome
upd(6)mat, TS14, upd(16)mat, upd(20)mat
SRS, upd(6)mat, upd(20)mat
SRS, upd(6)mat, upd(16)mat
Major clinical and overlapping findings
53.8 % (7/13)
77 % (47/61)
58.8 % (20/34)
Abnormality: 8 %
Abnormality: 35 %
97 % (33/34)
33.3 % (2/6)
36.6 % (11/30)
2 % (1/49)
(6.7 % (2/30)
43.8 % (153/349)
33.3 % (126/378
44 % (54/123)
94 % (379/403)
7 % (3/35)
45 % (n = 143) 
abdominal wall defects
21 % (24/114)
62.3 % (250/401)
Omphalocele: 32.3 % (11(34)
Exomphalos: 56.8 % (142/250)
diastasis recti: 67.6 % (23/34)
TNDM: 100 %
Hypoglycemia: 24 %
Hypoglycemia: 19 %; diabetes type 2 reported in later life
Hypoglycemia: 43.4 % (162/373)
Hypoglycemia diabetes type 2 reported in later life
Diabetes type 2: 25 %
4 % 
Global delay: 65 %
Global delay: 20 %
50 % (7/14)
76 % (26/34)
Increased sensitivity to heat
40-80 % 
Reported in later life 
dysmorphic/typical facial gestalt
18 % (21/114)
14.2 % (6/49)
8 % (9/116)
Low set posterior
Low set posterior
61.8 % (230/372)
17.6 % (9/51)
9 % (10/114)
5-10 % 
Currently, nine IDs have been described, but there are certainly more: In addition to the generally accepted paediatric IDs and the specific precocious puberty entity, there are three further molecular disturbances in discussion to represent separate IDs (upd(6)mat, upd(16)mat, upd(20)mat).
Transient neonatal diabetes mellitus type 1
Transient neonatal diabetes mellitus type type 1 (TNDM1) is characterised by intrauterine growth retardation (IUGR) and hyperglycaemia in infancy. The diabetes mellitus typically develops in the first weeks of life and resolves by the age of 18 months; however, it is growing clear that individuals with TNDM are at risk of relapse, in adolescence or early adulthood, with type 2 diabetes [16, 17]. Aside from these features, TNDM1 has no major cardinal features; however, individuals may have congenital abnormalities . Macroglossia (large tongue) affects just under half of infants with TNDM1, and about one in five individuals may also have a minor anomaly of the abdominal wall. Other congenital problems are rare and may be associated with MLID rather than TNDM per se. Approximately 10 % of individuals with TNDM1 do not present with hyperglycaemia at birth .
TNDM is associated with an overexpression of PLAGL1/ZAC in 6q24 (Fig. 1), a maternally imprinted gene. It encodes a zinc finger protein which binds DNA and hence influences the expression of other genes (for review, .
SRS is a clinically and molecularly heterogeneous growth retardation syndrome. Apart from pre- and postnatal growth failure, the major features include a relative macrocephaly at birth, a typical facial gestalt (protruding forehead, triangular face), body asymmetry, and feeding difficulties in infancy. Furthermore, first follow-up data indicate a risk for adult-onset diseases . The clinical presentation is variable and at least in part influenced by the mosaic distribution of molecular changes , but several scoring systems have been suggested . Approximately 10 % of SRS patients have maternal UPD for chromosome 7 (upd(7)mat) or segmental upd(7q)mat (for review, [24, 25]) (Fig. 2). The majority of patients carry molecular changes in 11p15, the most prevalent (~40 %) being hypomethylation of H19/IGF2: IG DMR (Fig. 3). Additionally, numerous (submicroscopic) disturbances of chromosomes 7 and 11 as well as of other chromosomes have been described; thus screening for cryptic genomic imbalances is indicated after exclusion of upd(7)mat and 11p15 epimutations [26, 27]. The genes causing the SRS phenotype on chromosomes 7 and 11 are currently unknown, but evidences for a role of IGF2 and CDKN1C in 11p15.5 and MEST in 7q32 have been reported [9, 28–30].
BWS was initially called EMG syndrome from its three main features of exomphalos, macroglossia and (neonatal) gigantism. The clinical diagnosis of BWS is often difficult due to its variable presentation and the phenotypic overlap with other overgrowth syndromes (for review, [31–33]) and isolated hemihypertrophy. In 5–7 % of children, embryonal tumours (most commonly Wilms tumour) are diagnosed.
In nearly 80 % of BWS patients chromosome 11p15.5 epimutations or mutations (Fig. 4), involving multiple loci, can be detected (including the ICR1 and KCNQ1OT1: TSS DMR DMRs)(for review, ). Most BWS cases are sporadic but familial inheritance is observed in up to 15 % of all cases. Microdeletions/duplications or point mutations at the ICRs are usually found in familial BWS with aberrant 11p15 methylation; for example, deletions and point mutations of OCT4/SOX4 binding sites in H19/IGF2: IG DMR are associated with H19/IGF2: IG DMR hypermethylation [5, 35, 36]. Conversely, CDKN1C mutations are frequent in familial cases with normal 11p15 methylation . These BWS pedigrees resemble that of an autosomal dominant inheritance but with parent-of-origin dependent effects on penetrance. Most cases of BWS with an KCNQ1OT1: TSS DMR epimutation are sporadic but there is an association with assisted reproductive technologies . Robust genotype/epigenotype-phenotype correlations have been established for BWS [35, 39, 40]: hemihypertrophy is strongly associated with upd(11)pat, exomphalos with KCNQ1OT1: TSS DMR hypomethylation and CDKN1C mutations, and, most importantly, the risk of Wilms tumour is significantly increased in H19/IGF2: IG DMR hypermethylation and upd(11)pat in comparison to the other molecular subgroups. By contrast, other embryonic tumors such as neuroblastoma and adrenal tumors are observed in patients with KCNQ1OT1: TSS DMR or upd(11)pat but at a much lower incidence. Hence, the determination of the molecular subtype is important for an individual prognosis and management. Nevertheless, the phenotypic transitions are fluid and testing for all molecular subtypes should be offered in patients with BWS features.
Temple syndrome (TS14) was first described in 1991 in a patient with a maternal UPD of chromosome 14 , and after it turned out that it is a recognizable phenotype the name upd(14)mat syndrome was suggested. Meanwhile, other molecular changes have been reported as well [42, 43]; therefore, the name TS14 has been proposed  (Fig. 5). TS14 is mainly characterised by prenatal and postnatal growth retardation, muscular hypotonia, feeding difficulties in early childhood, truncal obesity and early onset of puberty. TS14 patients show clinical features overlapping with PWS and SRS; thus, screening for chromosome 14q32 should be performed in patients with PWS- and SRS-like phenotypes after exclusion of the specific (epi)mutations. For TS14 the role of an altered RTL1 and DLK1 expression has been suggested .
The second recently defined ID is KOS14 which is mainly characterised by polyhydramnios, placentomegaly, excessive birth weight, a unique facial appearance with full cheeks and protruding philtrum, distinctive chest roentgenograms with coathanger rips and a bell-shaped thorax, abdominal wall defects (omphalocele, diastasis recti), variable developmental delay and/or intellectual disability, poor sucking usually requiring gastric tube feeding, hepatoblastoma and a mortality rate of 20–25 % in the neonate period .
Known causes of KOS are upd(14)pat (~65 %), epimutations affecting the MEG3/DLK: IG DMR and the MEG3: TSS DMR (~15 %) and microdeletions involving the MEG3/DLK: IG DMR and/or the MEG3: TSS DMR (~20 %) (Fig. 6). The detailed characterisation of KOS14 with deletions of different sizes has allowed the deciphering of the regulation mechanism in the 14q32 imprinted region [11, 46]: whereas deletion of the MEG3/DLK: IG DMR is associated with both the clinical KOS14 phenotype and placental abnormalities, carriers of deletions restricted to the MEG3: TSS DMR do not show placental abnormalities. It has been postulated that the increased expression of RTL1 is responsible for the clinical outcome, whereas a role of DLK1 can be neglected .
A clinical diagnosis of AS demands fulfilment of four major criteria and minimum three of the six minor criteria. The major criteria are severe developmental delay, movement or balance disorder, severe limitations in speech and language and typical abnormal behavior including happy demeanor and excessive laughter. The six minor criteria are postnatal microcephaly, seizures, abnormal EEG, sleep disturbance, attraction to or fascination with water, and drooling . The unique clinical features do not usually manifest within the first year of life, but developmental delay is noticed around 6 months of age. In about 10 % of the individuals with a clinical diagnosis of AS it is not possible to find the underlying genetic mechanism and other diagnoses should be considered. AS can be caused by maternally derived de novo deletion of 15q11-q13 (70–75 %), paternal uniparental disomy (upd(15)pat) of chromosome 15 (3–7 %) or an imprinting defect (2–3 %) all of which lead to lack of expression of maternally expressed 15q11-q13 genes (Fig. 7). Furthermore, mutations in UBE3A also cause Angelman syndrome (10–15 %). Imprinting defects can either be due to primary imprinting epimutations without DNA sequence alterations or due to deletions in the imprinting centre (IC) critical region (AS-SRO) [48, 49]. The 15q11-q13 chromosomal region contains imprinted genes, some of which are exclusively expressed from either of the parental alleles. Two exclusively maternally expressed genes, UBE3A and ATP10A, are located with this region: UBE3A encodes an E3 ubiquitin-protein ligase which is expressed exclusively from the maternal allele in human foetal brain and in adult frontal cortex [50, 51]. AS can be caused either by lack of UBE3A expression or by mutations in UBE3A. The role of the other imprinted gene, ATP10A, is however unclear. In individuals with deletions, UPD or imprinting defects, ATP10A expression is lacking, but in individuals with point mutations in UBE3A it is left unaffected.
PWS is clinically characterised by severe hypotonia and feeding difficulties in early infancy, followed by excessive eating and development of morbid obesity in later infancy or early childhood. Cognitive impairment is seen in almost all individuals but varies in severity. A behavioral phenotype with temper tantrums, stubbornness, manipulative behavior and obsessive-compulsive disorder is constant. Hypogonadism in both males and females may cause genital hypoplasia and incomplete pubertal development; and most individuals are infertile. Short stature, and small hands and feet are common features. Characteristic facial features, strabismus and scoliosis are often present. Clinical diagnostic criteria for PWS have been developed [52, 53]; however, confirmation of the clinical diagnosis with molecular genetic testing is required.
PWS is caused by lack of expression of the paternally contributed 15q11-q13 genes. There are three mechanisms leading to PWS: deletion of the 15q11-q13 imprinted loci on the paternal allele (75–80 %), maternal UPD of chromosome 15 (upd(15)mat) (20–25 %) and imprinting defects (<1 %) (Fig. 8). The common breakpoint for the deletions are the same as for AS. Imprinting defects can either be due to primary epimutations without DNA sequence alterations or it can be due to small deletions in the imprinting centre (IC) critical region (PWS-SRO) . The 15q11-q13 chromosomal region contains imprinted genes, some of which are exclusively expressed from either of the parental alleles. Paternally expressed genes are: MKRN3, MAGEL2, NDN, PWRN1, C15orf2, SNURF-SNRPN and several snoRNA genes (SNORD64, SNORD107, SNORD108, SNORD109A, SNORD109B, SNORD115 and SNORD116). SNORD115 and SNORD116 are present in 47 and 24 gene copies, respectively, whilst the other snoRNA genes are single copy genes. Deficiency of SNORD116 is thought to cause the key characteristics of the PWS phenotype [55, 56].
Puberty is a complex biological process involving sexual maturation and accelerated growth. These processes normally initiate when pulsatile secretion of gonadotropin-releasing hormone (GnRH) from the hypothalamus begins. Early activation of the hypothalamic-pituitary-gonadal axis results in gonadotropin-dependent precocious puberty (also known as central precocious puberty, CPP; development of secondary characteristics before the age of 8 year in girls and 9 years in boys). With the advent of advanced sequencing methods, exome-sequencing of familial cases of CPP have identified genetic defects in transcripts with no previous link to hypothalamic-pituitary-gonadal regulation. Loss-of-function mutations in the Makorin ring finger 3 (MKRN3) were initially identified in CPP families [57–60]. Consistent with the genes imprinting status the phenotype was only present upon paternal transmission of the mutation. Subsequently, mutations in MKRN3 have been shown to be the most frequent cause of familial CPP and they have also been detected in nearly 4 % in a cohort of 215 non-familial idiopathic CCP . The MKRN3 gene (also known as ZNF127) is an intronless transcript located on chromosome 15q11.2 in the PWS critical region, encoding for a protein with C3H zinc-finger and RING zinc-finger motifs. Unlike other imprinting disorders that can result from multiple mechanisms, it is currently unknown if CCP can arise from loss of MKRN3 expression due to deletion, segmental maternal uniparental disomy or an imprinting defect.
PHP is a group of disorders characterised by PTH resistance in the kidney, i.e. pseudohypoparathyroidism. Most cases of PHP belong to the type 1, i.e. are caused by genetic or epigenetic alterations at the imprinted GNAS locus. PHP1A comprises patients affected with resistance to PTH and TSH (and other GPCR proteins), and features of obesity and Albright hereditary osteodystrophy including short stature, brachydactyly, ectopic ossifications and mental retardation. PHP1A is caused by inactivating mutations in the maternal allele of the GNAS gene. Paternal GNAS mutations are associated with AHO, no hormonal resistance and no obesity, a constellation of features grouped under the term of pseudopseudohypoparathyroidism (PPHP) as well as with progressive osseous heteroplasia (POH). In contrast, the phenotype of most PHP1B patients is limited to renal PTH resistance  and in some cases, mild TSH resistance. Few patients with PHP1B display some features of Albright hereditary osteodystrophy . Patients with PHP1B share a loss of methylation at the A/B differentially methylated region (DMR) of GNAS, likely leading to the downregulated expression of the GNAS-Gsα transcript in imprinted tissues (Fig. 9). Some patients carry additional epigenomic changes along the GNAS locus. About 20 % of PHP1B are inherited and due to deletions of GNAS imprinting control regions. The remaining 80 % are sporadic. A small subset is due to paternal UPD of chromosome 20q, yet the vast majority are still of unknown cause (for review: ). Whilst obesity and short stature are long known features of PHP1A, it became only recently apparent that growth and metabolism are affected in both paternal and maternal (epi)genetic alterations of the GNAS locus [65, 66].
Despite the gaps in understanding their pathoaetiology and their clinical heterogeneity, the aforementioned IDs are meanwhile well established as they are associated with molecular changes in disease-specific loci. However, three further clinical entities have been suggested in which imprinted genes are known or suspected to be involved, and which might become IDs.
Maternal uniparental disomy of chromosome 6 (upd(6)mat)
Maternal UPD of chromosome 6 (upd(6)mat) has been hypothesized to be associated with intrauterine growth retardation: among the 13 cases reported so far, 7 revealed a IUGR (http://www.fish.uniklinikum-jena.de/UPD.html). Indeed, homozygosity of a recessive allele causing IUGR has been discussed as the pathogenic mechanism as many patients share an isodisomic region in 6q16qter. However, not all upd(6)mat carriers presenting IUGR share this region, in one case homozygosity of a recessive CUL7 has been identified causing 3 M syndrome, a growth retardation syndrome. However, it has been postulated that upd(6)mat might be regarded as a further imprinting disorder .
Maternal uniparental disomy of chromosome 16 (upd(16)mat)
Maternal UPD of chromosome 16 (upd(16)mat) is the most often reported UPD other than upd(15). This is not surprising since risk of UPD is much higher in chromosomes involved in aneuploidies and trisomy 16 is the most common autosomal trisomy in human abortions. Trisomy 16 itself is usually lethal in non-mosaic state in the fetus, but in trisomy rescue is compatible with life. As a consequence of UPD formation by trisomy rescue, many of the reported upd(16)mat cases are associated with trisomy 16 mosaicism in the placenta (for review, http://www.fish.uniklinikum-jena.de/UPD.html). The upd(16)mat has been suspected to have clinical consequences. However, the heterogeneity of the birth defects observed suggested that the phenotype might rather be influenced by placenta insufficiency than by the UPD itself . The possibility that upd(16)mat is associated with imprinting is difficult to assess due to the trisomy 16 mosaicism present in many cases. By an extensive clinical analysis of a series of mosaic trisomy 16 cases (n = 83) including upd(16)mat (n = 33), Yong et al.  concluded that upd(16)mat might be associated with more severe growth retardation in utero and an elevated risk of malformation. However, the role of imprinted genes on chromosome 16 contributing to the phenotype is unclear at the moment.
Maternal uniparental disomy of chromosome 20 (upd(20)mat)
Maternal uniparental disomy of chromosome 20 (upd(20)mat) has been reported in 12 patients , 3 of whom also had mosaicism for complete or partial trisomy of chromosome 20. All patients with upd(20)mat had intrauterine and postnatal growth retardation, and prominent feeding difficulties with failure to thrive often requiring gastric tube feeding in the first few years of life. No dysmorphisms or congenital abnormalities or major developmental delay have been reported. So far, other types of molecular alterations have not yet been reported, and a candidate region on chromosome 20 has not yet been defined. It is striking that these patients have not been described to have features reminiscent of paternal GNAS loss of function mutations, although the loss of the paternal GNAS allele (on chromosome 20) is associated with pre- and postnatal growth defect and Albright hereditary osteodystrophy . However, upd(20)mat probably presents a new imprinting disorder and its identification requires specialized molecular testing, which should be performed in patients with early-onset idiopathic isolated growth failure. In particular patients with a clinical diagnosis of SRS or TS14, but exclusion of their known molecular disturbances, are strong candidates for upd(20)mat as there appears to be significant phenotypic overlap.
The clinical and molecular overlap between IDs suggests that there may be causal links between them, either by shared causes of dysregulation affecting multiple imprinted genes, or by perturbation of interactions between the products of imprinted genes.
A growing number of ID patients have been reported to exhibit multilocus imprinting disturbance or MLID which can vary depending on the tissues studied [22, 71] (Table 1). Whilst the mechanisms associated with MLID are currently unknown, they all present with underlying aberrations in allelic DNA methylation. Indeed, evidence is growing that genomic mutations are involved in the etiology of MLID; known trans-acting factors include mutations in the ZFP57, the NLRP2 or the NLRP7 genes [72–75].
Another hypothesis which explains the clinical and molecular overlap between the different IDs is the “imprinted gene network” (IGN) . The existence of the IGN has been based on the observation of co-expression of imprinted transcript, as recently reported for the imprinted transcription factor PLAGL1, the gene responsible for TNDM . Changes in imprinted gene abundance occur due to increased transcription from the active allele in a DNA methylation independent fashion . Recently, additional gene networks have been described including the role of unoccupied insulin (IR) and insulin-like growth factor 1 receptor (IGF1R) signalling in the coordinated regulation of multiple imprinted genes associated with growth and development in mouse . Interestingly this regulation is independent of PLAGL1, despite this gene being downregulated by more than 80 % in the IR and IGF1R double knockout cells.
Finally the paternally expressed non-coding RNA IPW located in the commonly deleted chromosome 15 region in PWS regulates the levels of maternally expressed transcripts within the imprinted cluster on chromosome 14 . The transcriptional repression of the DLK1-DIO3 locus by IPW is due to altered repressive histone modifications at the IG-DMR, which is independent of DNA methylation, via targeted recruitment of the histone methyltransferase G9a. These observations support the reports of affected individuals with TS14 who display PWS-like phenotypes , enforcing the view that phenotypes associated with some IDs may be caused by aberrant expression of imprinted genes within other imprinted loci.
Recent rapid advances in the molecular and clinical pathogenesis of IDs have vividly illustrated the complexity of imprinting regulation, its vulnerability to genetic and epigenetic disturbance and its power as a paradigm of the interplay between genetics, epigenetics and phenotype. Identification of new mutational and epimutational pathways offers the potential for more precise molecular diagnosis and the development of new therapeutic regimes as the basis for a more directed and personalised medicine in IDs. At the same time, study of IDs may have impact beyond the borders of rare disorders, since they offer clear and tractable paradigms of the interplay between genetic, epigenetic and environmental variation upon human disorders spanning disturbances of growth and metabolism, diabetes and cancer.
All authors are members of the EUCID.net network, funded by COST (BM1208). TE is funded by the German Ministry of research and education (01GM1513B). GPdN is funded by I3SNS Program of the Spanish Ministry of Health (CP03/0064; SIVI 1395/09), Instituto de Salud Carlos III (PI13/00467) and Basque Department of Health (GV2014/111017).
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