C syndrome with skeletal anomalies, mental retardation, eyelid chalazion, Bitot’s spots and agenesis of the corpus callosum in an Egyptian child
Authors:
- Rabah M. ShawkyRSRabah M. Shawky
- Radwa GamalRGRadwa Gamal
Open Access
- 1 January 2017
- journal article
- Published by Springer Nature in Egyptian Journal of Medical Human Genetics
- Vol. 18 (1) , 93-97
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Trigonocephaly and Dandy walker variant in an Egyptian child – Probable mild Opitz trigonocephaly C syndromeEgyptian Journal of Medical Human Genetics, 2012
- Opitz trigonocephaly syndrome presenting with sudden unexplained death in the operating room: a case reportJournal of Medical Case Reports, 2011
- Mutations in CD96, a Member of the Immunoglobulin Superfamily, Cause a Form of the C (Opitz Trigonocephaly) SyndromeThe American Journal of Human Genetics, 2007
- New cases of Bohring–Opitz syndrome, update, and critical review of the literatureAmerican Journal of Medical Genetics Part A, 2006
- Severe end of Opitz trigonocephaly (C) syndrome or new syndrome?American Journal of Medical Genetics, 1999
- Syndromal and nonsyndromal primary trigonocephaly: Analysis of a series of 237 patientsAmerican Journal of Medical Genetics, 1998
- C syndrome and omphalocele: Another exampleAmerican Journal of Medical Genetics, 1992
- Opitz trigonocephaly syndromeAmerican Journal of Medical Genetics, 1991
- “C” trigonocephaly syndrome: Clinical variability and possibility of surgical treatmentAmerican Journal of Medical Genetics, 1990
- Further delineation of the C (trigonocephaly) syndromeAmerican Journal of Medical Genetics, 1981