Three patients resembling Teebi-Shaltout syndrome-Reference-Cited by-同舟云学术

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Three patients resembling Teebi-Shaltout syndrome

Published:2013-07 Issue: Volume: Page:n/a-n/a
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Aldemir Ozgur¹,Ozen Samim²,Erdem Sevcan³,Kiraz Aslihan¹,Akarsu Nurten⁴,Alanay Yasemin⁵

Affiliation:

1. Mersin Maternity and Children Hospital; Medical Genetic Department; Mersin; Turkey

2. Mersin Maternity and Children Hospital; Pediatric Endocrinology Department; Mersin; Turkey

3. Mersin Kadın Doğum ve Çocuk Hastanesi; Pediatric Cardiology Department; Mersin; Turkey

4. Hacettepe University; School of Medicine; Medical Genetic Department; Ankara; Turkey

5. Acibadem University; School of Medicine; Department of Pediatrics, Pediatric Genetics Unit; Istanbul; Turkey

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36082/fullpdf

Reference5 articles.

1. Craniofacial anomalies, abnormal hair, camptodactyly, and caudal appendage (Teebi-Shaltout syndrome): Clinical and autopsy findings;Froster;Am J Med Genet,1993

2. Blepharophimosis, blepharoptosis, defects of the anterior chamber of the eye, caudal appendage, radioulnar synostosis, hearing loss and umbilical anomalies in sibs: 3MC syndrome;Leal;Am J Med Genet Part A,2008

3. A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with growth failure, lip/palate cleft(s), and urogenital anomalies;Malpuech;Am J Med Genet,1983

4. Craniofacial anomalies, abnormal hair, camptodactyly, and caudal appendage;Teebi;Am J Med Genet,1989

5. Michels syndrome, Carnevale syndrome, OSA syndrome, and Malpuech syndrome: Variable expression of a single disorder (3MC syndrome);Titomanlio;Am J Med Genet Part A,2005

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