Publication: ALX4 related parietal foramina mimicking encephalocele in prenatal period
Program
KU-Authors
KU Authors
Co-Authors
Sivrikoz, Tuğba Saraç
Altunoğlu, Umut
Kalelioğlu, İbrahim Halil
Yüksel, Atıl
UyGüner, Oya Zehra
Has, Recep
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N/A
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Alternative Title
Abstract
What's Already Known About This Topic? PFM is an autosomal dominantly inherited genetic condition, caused by mutations in ALX4 and MSX2 genes. Reports on prenatally diagnosed cases are rare, and encephalocele remains the most leading differential diagnosis. What Does This Study Add? The full clinical spectrum of autosomal dominant ALX4-related PFM in affected family members can be demonstrated through identification of a prenatal case, by close collaboration of perinatologists and clinical geneticists, as in the four generation family reported herein. © 2016 John Wiley & Sons, Ltd.
Source
Publisher
Wiley-Blackwell
Subject
Genetics, Clinical genetics, Prenatal diagnosis, Gynecology
Citation
Has Part
Source
Prenatal Diagnosis
Book Series Title
Edition
DOI
10.1002/pd.4826
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