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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Autors principals:	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
Format:	Artigo
Idioma:	Russo
Publicat:	Union of pediatricians of Russia 2016-08-01
Col·lecció:	Педиатрическая фармакология
Matèries:	lysosomic acid lipase deficiency wolman disease cholesterol ester storage disease diagnosing differential diagnosis clinical course treatment enzyme replacing therapy children.
Accés en línia:	https://www.pedpharma.ru/jour/article/view/1422
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