Exercise Intolerance, Malnutrition, Abnormal Sweat Chloride Levels, and Two CFTR Mutations: Is It Cystic Fibrosis?

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Bibliographische Detailangaben
Veröffentlicht in:	Journal of pediatric health care 2015-03, Vol.29 (2), p.201-204
Hauptverfasser:	Com, Gulnur, MD, Uc, Aliye, MD
Format:	Artikel
Sprache:	eng
Schlagworte:	Adrenal Hyperplasia, Congenital - diagnosis Adrenal Hyperplasia, Congenital - physiopathology adrenal insufficiency Advanced Practice Nursing Anti-Inflammatory Agents - therapeutic use Blood Gas Analysis Child Cystic fibrosis Cystic Fibrosis - diagnosis Cystic Fibrosis Transmembrane Conductance Regulator - genetics Cystic Fibrosis Transmembrane Conductance Regulator - metabolism Diagnosis, Differential Exercise Test - methods Humans Hydrocortisone - therapeutic use Hypogonadism - diagnosis Hypogonadism - physiopathology Male Malnutrition - etiology Malnutrition - physiopathology Mutation Nursing Pediatrics Sweat - chemistry sweat chloride test Treatment Outcome
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