Literature DB >> 9001669

Achondroplasia in Sweden caused by the G1138A mutation in FGFR3.

A Alderborn1, M Anvret, K H Gustavson, L Hagenäs, C Wadelius.   

Abstract

Achondroplasia, an autosomal dominant inherited disorder, is one of the most common forms of skeletal dysplasia resulting in disproportionate extreme shortness. Recently, two point mutations, both affecting nucleotide 1138 in the fibroblast growth factor receptor type 3 (FGFR3) gene, were found to be the cause of the disorder. We investigated DNA from 16 Swedish patients with achondroplasia for the presence of these mutations. All patients were found to be heterozygous for the G to A transition at nucleotide 1138. Our data thus support previous reports showing a striking genetic homogeneity, in that almost all achondroplasia patients have the FGFR3 G380R mutation at the protein level.

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Year:  1996        PMID: 9001669     DOI: 10.1111/j.1651-2227.1996.tb13963.x

Source DB:  PubMed          Journal:  Acta Paediatr        ISSN: 0803-5253            Impact factor:   2.299


  1 in total

1.  Diagnostic, treatment and outcome possibilities in achondroplasia.

Authors:  Simona Bucerzan; Camelia Alkhzouz; Mirela Crisan; Diana Miclea; Carmen Asavoaie; Roxana Ilies; Paula Grigorescu-Sido
Journal:  Med Pharm Rep       Date:  2021-08-10
  1 in total

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