[Difficulties in diagnosis of cystic fibrosis]. / Trudnosci w rozpoznaniu mukowiscydozy.
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.
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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