| Literature DB >> 22992393 |
Ling-Chun Liu1, Shyh-Dar Shyur2, Szu-Hung Chu1, Li-Hsin Huang1, Yu-Hsuan Kao1, Wei-Te Lei1, Chieh-Han Cheng1, Chia-Yi Lo1, Chen-Kuan Chen1, Li-Ching Fang1.
Abstract
Cystic fibrosis (CF) is one of the most common autosomal recessive inherited disorders among Caucasians. Comparatively, it is considered to be a rare disease among Asians. To date, only a few cases of Taiwanese CF have been published. We report four CF cases from three families. Case 1 was the first report of CF associated with a homozygosity for the CF transmembrane conductance regulator gene (CFTR gene) mutation 3849+10kb C->T in a Taiwanese patient. Cases 2 and 3 had heterozygous c. 1898+5 G->T and heterozygous p. I1023R (novel mutation) for the CFTR gene mutation. Case 4 was homozygous for the CFTR gene mutation R553X being reported in 2005 and complicated with cor pulmonale. These four patients had received 300 mg bid aerosolized tobramycin treatment every other month.Entities:
Keywords: Cystic fibrosis; Cystic fibrosis transmembrane conductance regulator gene (CFTR gene); Taiwan
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Year: 2012 PMID: 22992393 DOI: 10.1016/j.jmii.2012.06.005
Source DB: PubMed Journal: J Microbiol Immunol Infect ISSN: 1684-1182 Impact factor: 4.399