Partial monosomy 13q
Encyclopedia
Partial Monosomy of chromosome 13q, can be defined as the loss of or physical deletion of the long arm of chromosome 13 in human beings. This is a rare genetic disorder which can result in unusual abnormalities in which the sufferer most often dies at an improbable age. There are other symptoms, not limiting to the ones listed below. The chances of a subject being born with this disorder is very low.

Symptoms

Partial Monosomy of the Long Arm of Chromosome 13 is the "deletion" or tearing off of the end of the long arm of chromosome thirteen in humans.

Problems/Symptoms have been noted to be:

Low birth weight

Malformations of the head

Abnormal eyes

Defects of the hands and feet, polydactyly
Polydactyly
Polydactyly or polydactylism , also known as hyperdactyly, is a congenital physical anomaly in humans, dogs, and cats having supernumerary fingers or toes....



Reproductive abnormalities (males)

and largely, psychological and motor abilities are retarded.

External Reading and Reference

http://www.bchealthguide.org/kbase/nord/nord643.htm NORD Database, on BcHealthGuide.org
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