Two brothers with the Marden-Walker syndrome: case report and review
- 1 February 1981
- journal article
- case report
- Published by BMJ in Journal of Medical Genetics
- Vol. 18 (1) , 50-53
- https://doi.org/10.1136/jmg.18.1.50
Abstract
Two brothers with blepharophimosis, congenital joint contractures, and mental retardation characteristic of the Marden-Walker syndrome are described. This sib pair strengthens the case for autosomal recessive inheritance of the syndrome.Keywords
This publication has 10 references indexed in Scilit:
- Zollinger-Ellison Syndrome With Marden-Walker SyndromeAmerican Journal of Diseases of Children, 1979
- The Marden-Walker syndrome.Journal of Medical Genetics, 1978
- Probable Marden-Walker syndrome: evidence for autosomal recessive inheritance.1975
- A child with facial and skeletal dysmorphia reminiscent of Schwartz syndrome.1975
- Marden-Walker syndrome.1975
- Congenital blepharophimosis, joint contractures, and muscular hypotoniaNeurology, 1971
- A New Generalized Connective Tissue SyndromeAmerican Journal of Diseases of Children, 1966
- Deux cas de malformations crânio-faciales: 1. Microphtalmie («nanisme oculo-palpébral») avec dysostose crânio-faciale et status dysraphique; 2. Dysmorphie mandibulo-oculo-faciale (syndrome d’Hallermann-Streiff)Ophthalmologica, 1964
- Congenital Blepharophimosis Associated with a Unique Generalized MyopathyArchives of Ophthalmology (1950), 1962
- Amyoplasia Congenita Causing Malpresentation of the FoetusBJOG: An International Journal of Obstetrics and Gynaecology, 1944