Literature DB >> 11598371

Molecular analysis of CYP-21 mutations for congenital adrenal hyperplasia in Singapore.

K Y Loke1, Y S Lee, W W Lee, L K Poh.   

Abstract

BACKGROUND: Congenital adrenal hyperplasia arising from 21-hydroxylase deficiency is associated with mutations in the CYP21 gene on chromosome 6p. This is the first report on the mutational spectrum of the CYP21 gene in Singapore.
METHODS: To catalogue the mutations, ten exons of the CYP21 gene from 28 Singaporean patients were analyzed by PCR amplification and direct sequencing.
RESULTS: Common mutations in descending order were the intron 2 splice site mutation (32.7% of the alleles), the I172N mutation (23.1% of the alleles), and the R356W mutation (19.2% of the alleles). Two potentially novel mutations were discovered: (1) duplication of 111 bp from codon 21 to codon 57 (exon 1) and (2) missense mutation (L261P, exon 7). There was generally a good genotype-phenotype correlation, allowing accurate prediction of the disease severity. Copyright 2001 S. Karger AG, Basel

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Year:  2001        PMID: 11598371     DOI: 10.1159/000049992

Source DB:  PubMed          Journal:  Horm Res        ISSN: 0301-0163


  9 in total

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6.  Clinical profile and inheritance pattern of CYP21A2 gene mutations in patients with classical congenital adrenal hyperplasia from 10 families.

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  9 in total

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