Literature DB >> 3425602

X-linked hydrocephalus.

P J Willems1, O F Brouwer, I Dijkstra, J Wilmink.   

Abstract

We report on a family with X-linked hydrocephalus: progressive increase in head circumference (OFC) led to the diagnosis in 3 patients; however, in 5 with normal OFC, the initial diagnosis had been "nonspecific" mental retardation, until identification of relatedness between 3 macrocephalic boys suggested segregation of a major Mendelian gene. Moderate to severe hydrocephaly was present in all macrocephalic patients and in 3 of the 5 with normal OFC, but CT-scan of the brain did not show aqueductal stenosis in any of them. We stress the importance of a brain CT-scan in every male with "nonspecific" mental retardation, especially in cases with X-linked inheritance, because confirmation of X-linkage has important genetic counseling consequences.

Entities:  

Mesh:

Year:  1987        PMID: 3425602     DOI: 10.1002/ajmg.1320270419

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  20 in total

1.  MASA syndrome (a form of complicated spastic paraplegia) and X linked hydrocephalus: variable expression of the same mutation at Xq28? Call for families.

Authors:  C Schrander-Stumpel; J Fryns; J J Cassiman; E Legius; A Spaepen; C J Höweler
Journal:  J Med Genet       Date:  1992-03       Impact factor: 6.318

2.  Further localization of X-linked hydrocephalus in the chromosomal region Xq28.

Authors:  P J Willems; L Vits; P Raeymaekers; J Beuten; P Coucke; J J Holden; C Van Broeckhoven; S T Warren; M Sagi; D Robinson
Journal:  Am J Hum Genet       Date:  1992-08       Impact factor: 11.025

Review 3.  X linked mental retardation.

Authors:  I A Glass
Journal:  J Med Genet       Date:  1991-06       Impact factor: 6.318

4.  A modifier locus on chromosome 5 contributes to L1 cell adhesion molecule X-linked hydrocephalus in mice.

Authors:  Alexis Tapanes-Castillo; Eli J Weaver; Robin P Smith; Yoshimasa Kamei; Tamara Caspary; Kara L Hamilton-Nelson; Susan H Slifer; Eden R Martin; John L Bixby; Vance P Lemmon
Journal:  Neurogenetics       Date:  2009-06-30       Impact factor: 2.660

Review 5.  X linked hydrocephalus and MASA syndrome.

Authors:  S Kenwrick; M Jouet; D Donnai
Journal:  J Med Genet       Date:  1996-01       Impact factor: 6.318

6.  Fetal hydrocephalus.

Authors:  Sergio Cavalheiro; Antonio Fernandes Moron; Carlos Gilberto Almodin; Italo Capraro Suriano; Vagner Hisaba; Patricia Dastoli; Mauricio Mendes Barbosa
Journal:  Childs Nerv Syst       Date:  2011-09-17       Impact factor: 1.475

7.  Refining the genetic location of the gene for X linked hydrocephalus within Xq28.

Authors:  M Jouet; E Feldman; J Yates; D Donnai; J Paterson; D Siggers; S Kenwrick
Journal:  J Med Genet       Date:  1993-03       Impact factor: 6.318

8.  A deletion of five nucleotides in the L1CAM gene in a Japanese family with X-linked hydrocephalus.

Authors:  T Takechi; J Tohyama; T Kurashige; K Maruta; K Uyemura; T Ohi; S Matsukura; N Sakuragawa
Journal:  Hum Genet       Date:  1996-03       Impact factor: 4.132

Review 9.  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

10.  The site of a missense mutation in the extracellular Ig or FN domains of L1CAM influences infant mortality and the severity of X linked hydrocephalus.

Authors:  R C Michaelis; Y Z Du; C E Schwartz
Journal:  J Med Genet       Date:  1998-11       Impact factor: 6.318

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