Publication: Type E Brachydactyly with Short Stature in a Mother and Her Two Daughters (a Case Report)
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Brakidaktili bir veya daha fazla metakarp ve/veya metatarsın asimetrik kısalığı ile karakterize bir parmak malformasyonudur. Çoğunlukla bir sendromun parçası olmakla birlikte otozomal dominant geçişlidir ve çeşitli şekillerde sınıflandırılır. Bilginturan ve ark. bir Türk ailesinde brakidaktili-kısa boy-hipertansiyon Sendromunu tanımladılar. Daha sonra Schuster ve ark. bu duruma neden olan genin 12p üzerinde olduğunu gösterdiler. Tip E brakidaktili'li hafif kısa boylu-normal zekalı-normal tansiyonlu bir anne ve iki kızı sunulmaktadır. Sitogenetik olarak bir anomali saptanmadı.
Type E brachydactyly is a digital malformation that characteristically causes an asymmetrical shortening of one or more metacarpals or metatarsals or both. Although commonly seen as part of a syndrome, it can be inherited as an autosomal dominant characteristic and has been classified into various patterns. Bilginturan et al firstly reported the brachydactyly-short stature-hypertension syndrome in a Turkish family. Schuster et al. mapped the gene causing this condition on 12p. We present a mother and her two daughters with mildly short stature-normal intelligence-normal blood pressure and Type E brachydactyly, and there was no chromosomal aberrations by using cytogenetical techniques
Type E brachydactyly is a digital malformation that characteristically causes an asymmetrical shortening of one or more metacarpals or metatarsals or both. Although commonly seen as part of a syndrome, it can be inherited as an autosomal dominant characteristic and has been classified into various patterns. Bilginturan et al firstly reported the brachydactyly-short stature-hypertension syndrome in a Turkish family. Schuster et al. mapped the gene causing this condition on 12p. We present a mother and her two daughters with mildly short stature-normal intelligence-normal blood pressure and Type E brachydactyly, and there was no chromosomal aberrations by using cytogenetical techniques
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Volume
18
Issue
3
Start Page
204
End Page
208
