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Revista Cubana de Pediatría

versão On-line ISSN 1561-3119

Resumo

DURAN ALVAREZ, Sandalio. Recessive autosomal polycystic disease. Rev Cubana Pediatr [online]. 2007, vol.79, n.2, pp. 0-0. ISSN 1561-3119.

Recessive autosomal and dominant autosomal polycystic kidney diseases are classically described as hereditary illnesses; they are also called polycystic disease of child type” and of adult typerespectively since both may be seen in any of these two life stages. The changing concepts of recessive autosomal disease, given the advances made in the treatment of newborns with this disease, and the location of the gen, the mutation of which causes it, encouraged us to make a brief literature review to help medical students and general practitioners to understand this disease.

Palavras-chave : recessive autosomal polycystic disease; congenital hepatic fibrosis; renal cysts.

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