Your browser doesn't support javascript.
loading
CFTR H609R mutation in Ecuadorian patients with cystic fibrosis.
Moya-Quiles, María Rosa; Glover, Guillermo; Mondéjar-López, Pedro; Pastor-Vivero, María Dolores; Fernández-Sánchez, Asunción; Sánchez-Solís, Manuel.
Afiliação
  • Moya-Quiles MR; Centro de Bioquímica y Genética Clínica, Hospital Virgen de la Arrixaca, El Palmar, Murcia, 30120, Spain. rosa.moya2@carm.es
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Mutação Puntual / Regulador de Condutância Transmembrana em Fibrose Cística / Fibrose Cística Idioma: En Ano de publicação: 2009 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Mutação Puntual / Regulador de Condutância Transmembrana em Fibrose Cística / Fibrose Cística Idioma: En Ano de publicação: 2009 Tipo de documento: Article