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Cystic fibrosis (CF) is autosomal recessive, genetic disorder cause of cystic fibrosis transmembrane regulatory (CFTR) gene mutation. CF often is observed in caucasian population. CFTR protein in cell apical membrane is canal responsible of transport sodium and clorid ions. Impaired sodium ion transport causes production viscous mucus. Disease include problems such as mucus, breathlessness and coughing. Blood glucose levels fluctuation are observed. This study aims comparison between lung function, functional capacity, muscle strength, physical activity, physical fitness and activities of daily living activities in cystic fibrosis with and without abnormal glucose tolerance
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The study aimed that comparison of clinical parameters in children with and without abnormal glucose tolerance in Cystic fibrosis.
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For the control group
Exclusion criteria
Patients having following disease
40 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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