Literature DB >> 7920660

MASA syndrome is due to mutations in the neural cell adhesion gene L1CAM.

L Vits1, G Van Camp, P Coucke, E Fransen, K De Boulle, E Reyniers, B Korn, A Poustka, G Wilson, C Schrander-Stumpel.   

Abstract

MASA syndrome is a recessive X-linked disorder characterized by mental retardation, adducted thumbs, shuffling gait, aphasia and, in some cases, hydrocephalus. Since it has been shown that X-linked hydrocephalus can be caused by mutations in L1CAM, a neuronal cell adhesion molecule, we performed an L1CAM mutation analysis in eight unrelated patients with MASA syndrome. Three different L1CAM mutations were identified: a deletion removing part of the open reading frame and two point mutations resulting in amino acid substitutions. L1CAM, therefore, harbours mutations leading to either MASA syndrome or HSAS, and might be frequently implicated in X-linked mental retardation with or without hydrocephalus.

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Year:  1994        PMID: 7920660     DOI: 10.1038/ng0794-408

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  33 in total

1.  Clinical mutations in the L1 neural cell adhesion molecule affect cell-surface expression.

Authors:  H D Moulding; R L Martuza; S D Rabkin
Journal:  J Neurosci       Date:  2000-08-01       Impact factor: 6.167

2.  X-linked mental retardation with seizures and carrier manifestations is caused by a mutation in the creatine-transporter gene (SLC6A8) located in Xq28.

Authors:  Kimberly A Hahn; Gajja S Salomons; Darci Tackels-Horne; Tim C Wood; Harold A Taylor; Richard J Schroer; Herbert A Lubs; Cornelis Jakobs; Rick L Olson; Kenton R Holden; Roger E Stevenson; Charles E Schwartz
Journal:  Am J Hum Genet       Date:  2002-03-15       Impact factor: 11.025

Review 3.  X linked hydrocephalus and MASA syndrome.

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

4.  The Arg-Gly-Asp motif in the cell adhesion molecule L1 promotes neurite outgrowth via interaction with the alphavbeta3 integrin.

Authors:  P M Yip; X Zhao; A M Montgomery; C H Siu
Journal:  Mol Biol Cell       Date:  1998-02       Impact factor: 4.138

5.  Five novel mutations in the L1CAM gene in families with X linked hydrocephalus.

Authors:  S M Gu; U Orth; A Veske; H Enders; K Klunder; M Schlosser; W Engel; E Schwinger; A Gal
Journal:  J Med Genet       Date:  1996-02       Impact factor: 6.318

6.  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

7.  Hydrocephalus and Hirschsprung's disease in a patient with a mutation of L1CAM.

Authors:  N Okamoto; Y Wada; M Goto
Journal:  J Med Genet       Date:  1997-08       Impact factor: 6.318

8.  A new mutation of the L1CAM gene in an X-linked hydrocephalus family.

Authors:  S Izumoto; M Yamasaki; N Arita; S Hiraga; T Ohnishi; K Fujitani; S Sakoda; T Hayakawa
Journal:  Childs Nerv Syst       Date:  1996-12       Impact factor: 1.475

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

Authors:  M Jouet; L Strain; D Bonthron; S Kenwrick
Journal:  J Med Genet       Date:  1996-03       Impact factor: 6.318

10.  Ninjurin2, a novel homophilic adhesion molecule, is expressed in mature sensory and enteric neurons and promotes neurite outgrowth.

Authors:  T Araki; J Milbrandt
Journal:  J Neurosci       Date:  2000-01-01       Impact factor: 6.167

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