Literature DB >> 8728703

Discordant segregation of Xq28 markers and a mutation in the L1 gene in a family with X linked hydrocephalus.

M Jouet1, L Strain, D Bonthron, S Kenwrick.   

Abstract

X linked recessive hydrocephalus is the most common hereditary form of hydrocephalus. Genetic analysis indicates that the majority of cases are caused by mutations in a single gene in Xq28, recently identified as the gene for neural cell adhesion molecule L1. Genetic heterogeneity for this disorder was suggested following the description of a single large pedigree where X linked hydrocephalus showed lack of linkage to Xq28 markers flanking the L1 gene. Mutation analysis in this family shows a single base pair deletion within the coding sequence of the L1 gene that would result in truncation of the mature protein. The nature of the mutation and its segregation with the disease through the pedigree indicate that it is the cause of X linked hydrocephalus in this family. These results are at odds with data obtained through segregation of alleles for markers flanking the L1 gene. Somatic and germline mosaicism is the most plausible explanation for these data, which also provide further evidence for genetic homogeneity of X linked hydrocephalus.

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Year:  1996        PMID: 8728703      PMCID: PMC1051879          DOI: 10.1136/jmg.33.3.248

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  19 in total

1.  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

2.  Aberrant splicing of neural cell adhesion molecule L1 mRNA in a family with X-linked hydrocephalus.

Authors:  A Rosenthal; M Jouet; S Kenwrick
Journal:  Nat Genet       Date:  1992-10       Impact factor: 38.330

3.  A missense mutation confirms the L1 defect in X-linked hydrocephalus (HSAS)

Authors:  M Jouet; A Rosenthal; J MacFarlane; S Kenwrick; D Donnai
Journal:  Nat Genet       Date:  1993-08       Impact factor: 38.330

4.  A duplication in the L1CAM gene associated with X-linked hydrocephalus.

Authors:  G Van Camp; L Vits; P Coucke; S Lyonnet; C Schrander-Stumpel; J Darby; J Holden; A Munnich; P J Willems
Journal:  Nat Genet       Date:  1993-08       Impact factor: 38.330

5.  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

6.  Identification of a 5' splice site mutation in intron 4 of the L1CAM gene in an X-linked hydrocephalus family.

Authors:  P Coucke; L Vits; G Van Camp; F Serville; S Lyonnet; S Kenwrick; A Rosenthal; M Wehnert; A Munnich; P J Willems
Journal:  Hum Mol Genet       Date:  1994-04       Impact factor: 6.150

7.  Genetic heterogeneity in X-linked hydrocephalus: linkage to markers within Xq27.3.

Authors:  L Strain; C M Gosden; D J Brock; D T Bonthron
Journal:  Am J Hum Genet       Date:  1994-02       Impact factor: 11.025

8.  X-linked spastic paraplegia (SPG1), MASA syndrome and X-linked hydrocephalus result from mutations in the L1 gene.

Authors:  M Jouet; A Rosenthal; G Armstrong; J MacFarlane; R Stevenson; J Paterson; A Metzenberg; V Ionasescu; K Temple; S Kenwrick
Journal:  Nat Genet       Date:  1994-07       Impact factor: 38.330

9.  The gene for X-linked hydrocephalus maps to Xq28, distal to DXS52.

Authors:  S Lyonnet; A Pelet; G Royer; O Delrieu; F Serville; B le Marec; A Gruensteudel; R A Pfeiffer; M L Briard; C Dubay
Journal:  Genomics       Date:  1992-10       Impact factor: 5.736

10.  Mutations in L1-CAM in two families with X linked complicated spastic paraplegia, MASA syndrome, and HSAS.

Authors:  J C Ruiz; H Cuppens; E Legius; J P Fryns; T Glover; P Marynen; J J Cassiman
Journal:  J Med Genet       Date:  1995-07       Impact factor: 6.318

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  3 in total

1.  Outline structure of the human L1 cell adhesion molecule and the sites where mutations cause neurological disorders.

Authors:  A Bateman; M Jouet; J MacFarlane; J S Du; S Kenwrick; C Chothia
Journal:  EMBO J       Date:  1996-11-15       Impact factor: 11.598

2.  Extensive germinal mosaicism in a family with X linked myotubular myopathy simulates genetic heterogeneity.

Authors:  M C Vincent; C Guiraud-Chaumeil; J Laporte; S Manouvrier-Hanu; J L Mandel
Journal:  J Med Genet       Date:  1998-03       Impact factor: 6.318

Review 3.  L1CAM: a major driver for tumor cell invasion and motility.

Authors:  Helena Kiefel; Sandra Bondong; John Hazin; Johannes Ridinger; Uwe Schirmer; Svenja Riedle; Peter Altevogt
Journal:  Cell Adh Migr       Date:  2012-07-01       Impact factor: 3.405

  3 in total

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