|Classification and external resources|
Uniparental disomy (UPD) occurs when a person receives two copies of a chromosome, or of part of a chromosome, from one parent and no copies from the other parent. UPD can be the result of heterodisomy, in which a pair of non-identical chromosomes are inherited from one parent (an earlier stage meiosis I error) or isodisomy, in which a single chromosome from one parent is duplicated (a later stage meiosis II error). Because it may lead to the duplication of lethal recessive genes, isodisomy is potentially dangerous, while heterodisomy is essentially benign.
- When the child receives two (different) homologous chromosomes (inherited from both grandparents) from one parent, this is called an heterodisomic UPD. Heterodisomy (heterozygous) indicates a meiosis I error.
- When the child receives two (identical) replica copies of a single homologue of a chromosome, this is called an isodisomic UPD. Isodisomy (homozygous) indicates either a meiosis II or postzygotic chromosomal duplication.
Most occurrences of UPD result in no phenotypical anomalies. However, if the UPD causing event happens during meiosis II, the genotype may include identical copies of the uniparental chromosome (isodisomy), leading to the manifestation of rare recessive disorders. UPD should be suspected in an individual manifesting a recessive disorder, where only one parent is a carrier.
Uniparental inheritance of imprinted genes can also result in phenotypical anomalies. Though few imprinted genes have been identified, uniparental inheritance of an imprinted gene can result in the loss of gene function which can lead to delayed development, mental retardation, or other medical problems.
- The most well-known conditions include Prader-Willi syndrome and Angelman syndrome. Both of these disorders can be caused by UPD or other errors in imprinting involving genes on the long arm of chromosome 15.
- Other conditions, such as Beckwith-Wiedemann syndrome, are associated with abnormalities of imprinted genes on the short arm of chromosome 11.
- Chromosome 14 is also known to cause particular symptoms such as skeletal abnormalities, mental retardation and joint contractures among others.
- UPD has rarely been studied prospectively, with most reports either focusing on known conditions or incidental findings. It has been proposed that the incidence may not be as low as conceived, rather may be underreported.
All chromosomes (uniparental diploidy)
Occasionally, all chromosomes will be inherited from one parent. A molar pregnancy results from fertilization by two sperm or a duplicated single sperm into an egg with DNA (partial molar pregnancy) or without DNA (complete molar pregnancy). A complete molar pregnancy is diploid (uniparental) and a partial molar pregnancy is triploid. Neither condition ever results in a liveborn infant and there is an increased risk for choriocarcinoma.
The first clinical case of UPD was reported in 1988 and involved a girl with cystic fibrosis and unusually short stature who carried two copies of maternal chromosome 7. Since 1991, out of the 47 possible disomies, 29 have been identified among individuals ascertained for medical reasons. This includes chromosomes 2, 5–11, 13–16, 21 and 22.
Clinical features for disomy 14 Pre and postnatal growth retardation muscular hypotonia feeding problems motor delay small hands and feet precocious puberty Truncal obesity
- Robinson WP (May 2000). "Mechanisms leading to uniparental disomy and their clinical consequences". Bioessays 22 (5): 452–9. doi:10.1002/(SICI)1521-1878(200005)22:5<452::AID-BIES7>3.0.CO;2-K. PMID 10797485.
- Human Molecular Genetics 3. Garland Science. p. 58. ISBN 0-8153-4183-0.
- , Angelman Syndrome, Online Mendelian Inheritance in Man
- Bhatt, Arpan; Liehr, Thomas; Bakshi, Sonal R. (2013). "Phenotypic spectrum in uniparental disomy: Low incidence or lack of study". Indian Journal of Human Genetics 19 (3): 131–34. doi:10.4103/0971-6866.120819.
- Spence JE, Perciaccante RG, Greig GM, Willard HF, Ledbetter DH, Hejtmancik JF, Pollack MS, O'Brien WE, Beaudet AL (1988). "Uniparental disomy as a mechanism for human genetic disease". American Journal of Human Genetics 42 (2): 217–226. PMC 1715272. PMID 2893543.
- "Uniparental disomy". Department of Medical Genetics, University of British Columbia. Archived from the original on 2002-06-17.
- T. Liehr: Cases with uniparental disomy
This article incorporates public domain text from The U.S. National Library of Medicine