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[Difficulties in diagnosis of cystic fibrosis]. / Trudnosci w rozpoznaniu mukowiscydozy.
Zielezinska, L; Szaflarska-Szczepanik, A.
Afiliación
  • Zielezinska L; Katedry i Kliniki Pediatrii, Aleroglogii i Gastroenterologii Akademii Medycznej im. L. Rydygiera w Bydgoszczy.
Pol Merkur Lekarski ; 7(43): 43-4, 2000 Jan.
Article en Pl | MEDLINE | ID: mdl-10765653
In this study we have presented the diagnostic difficulties in a child with cystic fibrosis recognised basing on the clinical picture of the disease, together with two elevated values of sweat chloride tests. The diagnosis was confirmed by an identification of delta F 508 mutation on both cystic fibrosis chromosomes. Normal sweat test results in a first stage of diagnosis performed twice in a newborn period were a factor which delated the diagnosis.
Asunto(s)
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fibrosis Quística Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans / Newborn Idioma: Pl Revista: Pol Merkur Lekarski Asunto de la revista: MEDICINA Año: 2000 Tipo del documento: Article Pais de publicación: Polonia
Buscar en Google
Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fibrosis Quística Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans / Newborn Idioma: Pl Revista: Pol Merkur Lekarski Asunto de la revista: MEDICINA Año: 2000 Tipo del documento: Article Pais de publicación: Polonia