Co-occurrence of Carpenter syndrome and double outlet right ventricle

Carpenter syndrome (Acrocephalopolysyndactyly type 2, OMIM 201000) is a rarely seen autosomal recessive disorder. In addition to abnormalities such as acrocephaly, craniosynostosis, facial asymmetry, polydactyly and syndactyly, obesity, hypogonadism, mental retardation, and corneal opacity, it may f...

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Bibliographic Details
Main Authors: Osman Güvenç, Derya Çimen, Derya Arslan, İbrahim Güler
Format: Article
Language:English
Published: KARE Publishing 2017-07-01
Series:Türk Kardiyoloji Derneği Arşivi
Subjects:
Online Access:https://jag.journalagent.com/z4/download_fulltext.asp?pdir=tkd&un=TKDA-16040