Literature DB >> 8471217

Autosomal recessive congenital stenosis of aqueduct of Sylvius.

P Barros-Nuñes1, F Rivas.   

Abstract

Congenital hydrocephalus is an etiologically heterogeneous central nervous system malformation. Mendelian inheritance of stenosis of the aqueduct of Sylvius (SAS) accounts for almost 2% of all nonsyndromic forms. Among the monogenetic forms the great majority are X-linked. In this report we describe autosomal recessive transmission of SAS hydrocephalus in a high consanguinity family.

Entities:  

Mesh:

Year:  1993        PMID: 8471217

Source DB:  PubMed          Journal:  Genet Couns        ISSN: 1015-8146


  5 in total

Review 1.  Congenital hydrocephalus: nosology and guidelines for clinical approach and genetic counselling.

Authors:  C Schrander-Stumpel; J P Fryns
Journal:  Eur J Pediatr       Date:  1998-05       Impact factor: 3.183

Review 2.  Autosomal recessive hydrocephalus with aqueductal stenosis.

Authors:  M Castro-Gago; A Alonso; J Eirís-Puñal
Journal:  Childs Nerv Syst       Date:  1996-04       Impact factor: 1.475

Review 3.  Genetics of human hydrocephalus.

Authors:  Jun Zhang; Michael A Williams; Daniele Rigamonti
Journal:  J Neurol       Date:  2006-06-13       Impact factor: 4.849

4.  Compound heterozygous variants in the multiple PDZ domain protein (MPDZ) cause a case of mild non-progressive communicating hydrocephalus.

Authors:  Nesreen K Al-Jezawi; Aisha M Al-Shamsi; Jehan Suleiman; Salma Ben-Salem; Anne John; Ranjit Vijayan; Bassam R Ali; Lihadh Al-Gazali
Journal:  BMC Med Genet       Date:  2018-03-02       Impact factor: 2.103

5.  L1CAM mutation in association with X-linked hydrocephalus and Hirschsprung's disease.

Authors:  Sha-Ron Jackson; Yigit S Guner; Russell Woo; Linda M Randolph; Henri Ford; Cathy E Shin
Journal:  Pediatr Surg Int       Date:  2009-07-30       Impact factor: 1.827

  5 in total

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