Autor: |
Lubani MM; Department of Paediatrics, Farwania Hospital, Kuwait., Doudin KI, Sharda DC, Shaltout AA, al-Shab TS, Abdul Al YK, Said MA, Salhi MM, Ahmed SA |
Jazyk: |
angličtina |
Zdroj: |
European journal of pediatrics [Eur J Pediatr] 1989 Jan; Vol. 148 (4), pp. 333-6. |
DOI: |
10.1007/BF00444128 |
Abstrakt: |
Congenital chloride diarrhoea was diagnosed in 16 Kuwaiti children over a 7 year period (1980-1986) with an estimated incidence of 7.6 per 100,000 live births. The mean age at diagnosis was 3.2 months (range 1 week to 5 months). There were 9 boys and 7 girls with a mean age of 3 years 10 months (range 10 months to 7 years). All children had a shortened gestational period, abdominal distension and chronic diarrhoea. The serum electrolytes in all patients prior to treatment showed hyponatraemia, hypokalaemia, hypochloraemia and metabolic alkalosis. The diagnosis was confirmed by a stool chloride content that exceeded the sum of faecal sodium and potassium. Fifteen patients survived and showed catch-up growth with adequate replacement therapy and 1 died with renal failure. |
Databáze: |
MEDLINE |
Externí odkaz: |
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