Encyclopedia > Brachydactyly type a1

  Article Content

Brachydactyly

Redirected from Brachydactyly type a1

Brachydactyly is a genetic disease in which the middle phalanx of the fingers is missing. It is caused by being heterozygous for a certain gene. Homozygotes for that gene are born with severe skeletal malformations and do not survive.

Brachydactyly Type A1 Abnormal shortness of the fingers and toes. Inheritad as an autosomal dominant trait. Symptoms: extra carpals, short phalanges, short thumbs, short metacarpals, syphalangism of the fingers and 2nd and 3rd toes, short femurs, and sometimes ansent phalanges. Fatal during infancy because of major skeletal defects.



All Wikipedia text is available under the terms of the GNU Free Documentation License

 
  Search Encyclopedia

Search over one million articles, find something about almost anything!
 
 
  
  Featured Article
242

... 190s 200s 210s 220s 230s - 240s - 250s 260s 270s 280s 290s Years: 237 238 239 240 241 - 242 - 243 244 245 246 247 Events Patriarch Titus[?] succeeds ...

 
 
 
This page was created in 31.6 ms