[Mid-term outcome of 2 cases with maple syrup urine disease: role of liver transplantation in the treatment]. / Devenir à moyen terme de deux cas de leucinose: place de la transplantation hépatique dans le traitement.
Arch Pediatr
; 1(8): 730-4, 1994 Aug.
Article
en Fr
| MEDLINE
| ID: mdl-7842107
BACKGROUND: Dietary treatment of maple syrup urine disease remains difficult; chronic nutritional support in the child does not always avoid acute crises so that liver transplantation may represent an alternate choice in some cases. CASE REPORTS: Two gypsy cousins were born by an interval of 4 days; both had maple syrup urine disease and were similarly treated from the first days of life. They were given exchange transfusions followed by diet restricted in the branched chain amino acids, maintaining normal growth and plasma leucine concentrations under 7 mg/100 ml. Laura, at 10 years, was retarded at school. Compliance to school attendance was limited by her diet problems. Helen suffered at 7 yr 3 mo from liver failure due to hepatitis A virus infection which required liver transplantation. Protein intake was normal 1 week later. At 10 years, she presented with the same degree of school retardation as her cousin, and was placed in the same class. CONCLUSION: Liver transplantation may be effective for treating metabolic problems in MSVD without significative difference between outcome post classic treatment or post liver transplantation.
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Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Trasplante de Hígado
/
Enfermedad de la Orina de Jarabe de Arce
/
Discapacidad Intelectual
Tipo de estudio:
Observational_studies
/
Prognostic_studies
/
Risk_factors_studies
Límite:
Child
/
Female
/
Humans
Idioma:
Fr
Revista:
Arch Pediatr
Año:
1994
Tipo del documento:
Article
País de afiliación:
Francia
Pais de publicación:
Francia