Literature DB >> 2377348

Walker-Warburg syndrome. Case report and literature review.

K J Murphy1, R PeBenito, R L Storm, C Ferretti, D P Liu.   

Abstract

The Walker-Warburg syndrome (WWS) is a fatal dysmorphic disorder of unknown etiology, but strongly suggests an autosomal recessive mode of inheritance. It is characterized by severe congenital oculo-cerebral malformations (lissencephaly, congenital hydrocephalus, and ocular lesions). The authors report a case of WWS that occurred in a consanguineous union, with a review of the literature. Possible pathogenesis, and disorders sharing the features of WWS are discussed. Families-at-risk for WWS should be identified for prenatal diagnosis and for genetic counselling.

Entities:  

Mesh:

Year:  1990        PMID: 2377348     DOI: 10.3109/13816819009012954

Source DB:  PubMed          Journal:  Ophthalmic Paediatr Genet        ISSN: 0167-6784


  2 in total

1.  A novel pattern of oculocerebral malformation.

Authors:  B J Clark; W R Lee; D Doyle; R Arngrimsson; J L Tolmie; J B Stephenson
Journal:  Br J Ophthalmol       Date:  1997-06       Impact factor: 4.638

2.  Prenatal Diagnosis of Walker-Warburg Syndrome Using Single Nucleotide Polymorphism Array: A Clinical Experience from Three Related Palestinian Families with Congenital Hydrocephalus.

Authors:  Iman S Abumansour; Eman Al Sulmi; Bernard N Chodirker; Jennifer C Hunt
Journal:  AJP Rep       Date:  2015-04-27
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.