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[Niemann pick type A, a case report]
Journal of Mazandaran University of Medical Sciences. 2006; 16 (53): 112-118
en Persa | IMEMR | ID: emr-77902
ABSTRACT
Niemann Pick type A is a very rare hereditary disease with an incidence 1 in 20000-40000 live birth, which is calassified as a shingolipidoses. The disease is marked by the abnormal accumulation of sphingomyelin in most tissues, secondary to sphingomylinase deficiency. The most clinical manifestations are Splenohepatomegaly-cherry red maculae-neuropathologic findings. This is a case report of an infant with clinical manifestation of Niemann Pick disease type A
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Índice: IMEMR (Mediterraneo Oriental) Asunto principal: Esfingomielinas / Esplenomegalia / Hepatomegalia Tipo de estudio: Informe de Casos Límite: Humanos Idioma: Persa Revista: J. Mazandaran Univ. Med. Sci. Año: 2006

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Índice: IMEMR (Mediterraneo Oriental) Asunto principal: Esfingomielinas / Esplenomegalia / Hepatomegalia Tipo de estudio: Informe de Casos Límite: Humanos Idioma: Persa Revista: J. Mazandaran Univ. Med. Sci. Año: 2006