CFTR H609R mutation in Ecuadorian patients with cystic fibrosis.
J Cyst Fibros
; 8(4): 280-1, 2009 Jul.
Article
em En
| MEDLINE
| ID: mdl-19457724
Mutation epidemiology in each ethnic group is important for cystic fibrosis diagnosis and genetic counselling. To date, little has been reported on the prevalence of cystic fibrosis in the Ecuadorian population where the mutation distribution appears to differ from that of Europe. We present a series of four Ecuadorian patients homozygous for the H609R mutation in the CFTR gene. This is the first report of detection of this mutation in the Ecuadorian population. Taking advantage of the homozygous status of the patients, an evaluation of the most important clinical parameters is presented. From the diagnostic point of view, the information provided by our study is of relevance in designing an appropriate strategy for genetic testing of patients in Ecuador and in European countries where immigration from Ecuador is common.
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Mutação Puntual
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Regulador de Condutância Transmembrana em Fibrose Cística
/
Fibrose Cística
Idioma:
En
Ano de publicação:
2009
Tipo de documento:
Article