Chromosome 15q trisomy

Chromosome 15q trisomy

Chromosome 15q trisomy is an extremely rare genetic disorder, caused by a chromosomal aberration in which there is an excess copy of the long ("q") arm of human chromosome 15. The disorder is also known as Distal Duplication 15q and Partial Duplication 15q Syndrome.

The disorder is primarily characterized by growth abnormalities, which range from growth retardation to accelerated growth, mental retardation, and distinctive malformations of the head and face. Additional abnormalities may involve malformation of the skeleton, spine and neck; fingers and/or toes; genitals (particularly in males); and, in some cases, heart problems. When accelerated growth is present, it is thought to result from the duplication of the IGF1 receptor gene.

See also



Wikimedia Foundation. 2010.

Игры ⚽ Поможем написать курсовую

Look at other dictionaries:

  • Chromosome 15q partial deletion — is an extremely rare human genetic disorder, caused by a chromosomal aberration in which the long ( q ) arm of one copy of chromosome 15 is deleted, or partially deleted. If the mother s copy of the chromosomal arm is deleted, Angelman syndrome… …   Wikipedia

  • trisomy 15 — /ˌtraɪsəmi fɪfˈtin/ (say .truysuhmee fif teen) noun a chromosomal abnormality causing developmental impairment, intellectual disability, and physical abnormalities particularly of the head and face, caused by the presence of three q or long arms… …  

  • List of diseases (C) — A list of diseases in the English wikipedia.C* C syndrome * C1 esterase deficiency (angioedema)CaCac Cal* Cacchi Ricci disease * CACH syndrome * Cafe au lait spots syndrome * Caffey disease * CAHMR syndrome * Calcinosis cutis (see also CREST… …   Wikipedia

  • syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… …   Medical dictionary

  • Prader–Willi syndrome — Prader Willi syndrome Classification and external resources ICD 10 Q87.1 ICD 9 759.81 …   Wikipedia

Share the article and excerpts

Direct link
Do a right-click on the link above
and select “Copy Link”