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Familial 22q11.2 deletion syndrome with autosomal dominant inheritance

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10.17826-cutf.202658-206123.pdf (316.1Kb)
Date
2016
Author
Gokturk, Bahar
Gokdemir, Mahmut
Reisli, Ismail
Yildirim, Mahmut Selman
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Abstract
22q11.2 deletion syndrome is the most frequent microdeletion syndrome in humans and caused by hemizygote deletion on only one chromosome. Most of probands have a de novo deletion of 22q11.2, but 8-20% have inherited the 22q11.2 deletion from a parent (autosomal dominant mutation). Genotype-phenotype correlation is weak in this patient group. We aimed to present three members in the same family due to an autosomal dominant inheritance with 22q11.2 deletion and different clinical findings.
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https://dergipark.org.tr/tr/download/article-file/206123
http://hdl.handle.net/11727/3877
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  • Tıp Fakültesi / Faculty of Medicine [5092]
  • TR-Dizin İndeksli Yayınlar Koleksiyonu [993]
  • Wos İndeksli Yayınlar Koleksiyonu [4262]

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