Turkish infant with hypoelectrolytemia and metabolic alkalosis as sole manifestations of a mild form of cystic fibrosis (mutation D110H);Turkischer saugling mit hypoelektrolytamie und metabolischer alkalose als alleinige manifestation einer milden form der zystischen fibrose (mutation D110H)

Klinische Padiatrie

Volumn 212, Issue 1, 2000, Pages 41-43

  Weller, F ^a   Wiebicke, W ^a   Tummler B ^b  

^a Zentralkrankenhaus Bremen ^*  (Germany)

^b HANNOVER MEDICAL SCHOOL   (Germany)

Author keywords

Cystic fibrosis; Infant; Metabolic alkalosis; Molecular genetics

Indexed keywords

SODIUM CHLORIDE; ELECTROLYTE;

ARTICLE; CASE REPORT; CYSTIC FIBROSIS; DEHYDRATION; ELECTROLYTE DISTURBANCE; EXON; GENE MUTATION; HUMAN; HYPOCHLOREMIA; HYPOKALEMIA; HYPONATREMIA; INFANT; METABOLIC ALKALOSIS; MOLECULAR GENETICS; REHYDRATION; ALKALOSIS; BLOOD; DIFFERENTIAL DIAGNOSIS; ETHNOLOGY; GENETICS; GERMANY; HOSPITALIZATION; MALE; MENINGOENCEPHALITIS; METABOLISM; MUSCLE HYPOTONIA; MUTATION; NUCLEOTIDE SEQUENCE; POPULATION GENETICS; SWEAT; TURKEY (REPUBLIC);

ALKALOSIS; CYSTIC FIBROSIS; DIAGNOSIS, DIFFERENTIAL; DNA MUTATIONAL ANALYSIS; ELECTROLYTES; GENETICS, POPULATION; GERMANY; HUMANS; INFANT; MALE; MENINGOENCEPHALITIS; MUSCLE HYPOTONIA; MUTATION; SEVERITY OF ILLNESS INDEX; SODIUM CHLORIDE; SWEAT; TURKEY;

EID: 0034006015     PISSN: 03008630     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2000-9650     Document Type: Article

References (11)

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