Literature DB >> 1227520

Probable Marden-Walker syndrome: evidence for autosomal recessive inheritance.

S A Temtamy, A S Shoukry, M Raafat, S Mihareb.   

Abstract

Two first cousins, the offspring of consanguineous marriages, had features suggestive of Marden-Walker syndrome. Phenotypic similarities and differences for Schwartz-Jampel syndrome have been discussed. Main features of the Marden-Walker syndrome are failure to thrive, marked motor and mental retardation, and multiple malformations in the form of peculiar facies associated wilth poor muscle mass, mild congenital joint contractures, pigeon breast, kyphoscoliosis and arachnodactyly. Peculiar facies is due to blepharophimosis, congenital ptosis, hypoplastic mandible and low-set and malformed ears. Posterior median cleft of the palate as well as cardiac and renal anomalies were noted in the case reported by Marden and Walker. Our Case 2 had dextrocardia. The present report suggests autosomal recessive inheritance of this syndrome.

Entities:  

Mesh:

Year:  1975        PMID: 1227520

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN: 0547-6844


  3 in total

1.  Two brothers with the Marden-Walker syndrome: case report and review.

Authors:  F M Howard; P Rowlandson
Journal:  J Med Genet       Date:  1981-02       Impact factor: 6.318

2.  A 26-month-old child with Marden-Walker syndrome and pyloric stenosis.

Authors:  D Gossage; J M Perrin; M G Butler
Journal:  Am J Med Genet       Date:  1987-04

3.  The Marden-Walker syndrome.

Authors:  C R King; E Magenis
Journal:  J Med Genet       Date:  1978-10       Impact factor: 6.318

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.