In:
Pediatric pharmacology, Paediatrician Publishers LLC, Vol. 20, No. 4 ( 2023-08-22), p. 337-354
Abstract:
Lysosomal acid lipase deficiency is s a rare hereditary enzymopathy. The article presents epidemiological data and features of etiopathogenesis of two phenotypic forms of lysosomal acid lipase deficiency — Wolman disease and cholesterol ester storage disease. Special attention has been given to the key issues of differential diagnostic search, clinical guidelines based on the principles of evidence-based medicine have been given.
Type of Medium:
Online Resource
ISSN:
2500-3089
,
1727-5776
DOI:
10.15690/pf.v20i4.2602
Language:
Unknown
Publisher:
Paediatrician Publishers LLC
Publication Date:
2023
detail.hit.zdb_id:
3072851-4
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