Trigonocephaly and Dandy walker variant in an Egyptian child – Probable mild Opitz trigonocephaly C syndrome
Authors:
Open Access
- 29 February 2012
- journal article
- research article
- Published by Springer Nature in Egyptian Journal of Medical Human Genetics
- Vol. 13 (1) , 115-118
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- The Dandy–Walker variant: a case series of 24 pediatric patients and evaluation of associated anomalies, incidence of hydrocephalus, and developmental outcomesJournal of neurosurgery. Pediatrics, 2008
- Mutations in CD96, a Member of the Immunoglobulin Superfamily, Cause a Form of the C (Opitz Trigonocephaly) SyndromeThe American Journal of Human Genetics, 2007
- Antenatal diagnosis of deletion chromosome 11(q23-qter) (Jacobsen syndrome)Clinical Dysmorphology, 2007
- Opitz “C” trigonocephaly‐like syndrome in a patient with terminal deletion of 2p and partial duplication of 17qAmerican Journal of Medical Genetics Part A, 2004
- Diagnostic Practice and the Estimated Prevalence of Craniosynostosis in ColoradoArchives of Pediatrics & Adolescent Medicine, 1997
- FISH diagnosis of partial trisomy 13 and tetrasomy 13 in a patient with severe trigonocephaly (C) phenotypeAmerican Journal of Medical Genetics, 1994
- Orbital Teratoma Associated with TrigonocephalyPlastic and Reconstructive Surgery, 1991
- Trigonocephaly and the Opitz C syndrome.Journal of Medical Genetics, 1985
- Further delineation of the C (trigonocephaly) syndromeAmerican Journal of Medical Genetics, 1981
- The Dandy‐Walker syndromeNeurology, 1972