Deficiency of Lysosomic Acid Lipase: Clinical Recommendations for Child Health Care Delivery

The deficiency of lysosomic acid lipase is a rare hereditary enzymopathy. The focus of this article is the present condition of this issue. The authors demonstrate epidemiological data and etiopathogenetic features of two phenotypic forms of lysosomic acid lipase deficiency — Wolman disease and chol...

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Main Authors: A. A. Baranov, L. S. Namazova-Baranova, O. S. Gundobina, S. V. Mikhailova, E. U. Zakharova, E. A. Vishnyova, K. V. Savostianov, M. U. Stepanyan
Formato: Artigo
Idioma:Inglês
Publicado em: Paediatrician Publishers, LLC 2016-08-01
Colecção:Pediatričeskaâ Farmakologiâ
Assuntos:
lysosomic acid lipase deficiency
wolman disease
cholesterol ester storage disease
diagnosing
differential diagnosis
clinical course
treatment
enzyme replacing therapy
children.
Acesso em linha:https://www.pedpharma.ru/jour/article/view/1422
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