Literature DB >> 19685344

A novel L1CAM mutation in a fetus detected by prenatal diagnosis.

Maria Piccione1, Federico Matina, Marco Fichera, Mariangela Lo Giudice, Gianfranca Damiani, Maria Cristina Jakil, Giovanni Corsello.   

Abstract

X-linked hydrocephalus is due to mutations in the L1 neuronal cell adhesion molecule (L1CAM) gene. L1 protein plays a key role in neurite outgrowth, axonal guidance, and pathfinding during the development of the nervous system. We report on a familial case diagnosed by prenatal ultrasonographic examination, with cerebellar hypoplasia, agenesis of the corpus callosum, and the bilateral overlapping of the second and third fingers of the hand. Sequencing of the L1CAM gene showed a novel missense mutation in exon 14: transition of a guanine to cytosine at position 1777 (c.1777G>C), which led to an amino acid change of alanine to proline at position 593 (Ala593Pro) in the sixth immunoglobulin domain of the L1 protein. The L1CAM mutation testing should be considered in fetuses with ultrasonographic signs of hydrocephalus and a positive family history compatible with X-linked inheritance. We agree with previous reports that suggest also considering limb abnormalities other than adducted thumbs in addition to classical neurological disgenesis, as characteristic for L1-disease.

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Year:  2009        PMID: 19685344     DOI: 10.1007/s00431-009-1037-6

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  12 in total

Review 1.  Genetic and clinical aspects of X-linked hydrocephalus (L1 disease): Mutations in the L1CAM gene.

Authors:  S Weller; J Gärtner
Journal:  Hum Mutat       Date:  2001       Impact factor: 4.878

2.  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

3.  A novel L1CAM mutation with L1 spectrum disorders.

Authors:  Fatma Silan; Ismail Ozdemir; Willy Lissens
Journal:  Prenat Diagn       Date:  2005-01       Impact factor: 3.050

4.  Spectrum and detection rate of L1CAM mutations in isolated and familial cases with clinically suspected L1-disease.

Authors:  U Finckh; J Schröder; B Ressler; A Veske; A Gal
Journal:  Am J Med Genet       Date:  2000-05-01

5.  A new assay for the analysis of X-chromosome inactivation based on methylation-specific PCR.

Authors:  T Kubota; S Nonoyama; H Tonoki; M Masuno; K Imaizumi; M Kojima; K Wakui; M Shimadzu; Y Fukushima
Journal:  Hum Genet       Date:  1999-01       Impact factor: 4.132

6.  CRASH syndrome: mutations in L1CAM correlate with severity of the disease.

Authors:  M Yamasaki; P Thompson; V Lemmon
Journal:  Neuropediatrics       Date:  1997-06       Impact factor: 1.947

Review 7.  Neural cell recognition molecule L1: relating biological complexity to human disease mutations.

Authors:  S Kenwrick; A Watkins; E De Angelis
Journal:  Hum Mol Genet       Date:  2000-04-12       Impact factor: 6.150

8.  Expanding the phenotypic spectrum of L1CAM-associated disease.

Authors:  L Basel-Vanagaite; R Straussberg; M J Friez; D Inbar; L Korenreich; M Shohat; C E Schwartz
Journal:  Clin Genet       Date:  2006-05       Impact factor: 4.438

9.  Human non-synonymous SNPs: server and survey.

Authors:  Vasily Ramensky; Peer Bork; Shamil Sunyaev
Journal:  Nucleic Acids Res       Date:  2002-09-01       Impact factor: 16.971

10.  Neural adhesion molecule L1 as a member of the immunoglobulin superfamily with binding domains similar to fibronectin.

Authors:  M Moos; R Tacke; H Scherer; D Teplow; K Früh; M Schachner
Journal:  Nature       Date:  1988-08-25       Impact factor: 49.962

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