PMID: 8966098Mar 1, 1996Paper

Alpha-mannosidosis in two siblings

Pediatria polska
B DawydzikS Grałek

Abstract

A rare metabolic disease, alpha-mannosidosis, is described in two siblings. Psychomotoric deficiency, deafness, coarse face and radiological changes in the skeletal system indicated an inherited lysosomal storage disease.

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