患有沃尔曼病的婴儿的继发性噬血细胞性淋巴组织细胞增生症 - Suppr

Secondary Hemophagocytic Lymphohistiocytosis in an Infant with Wolman Disease.

作者信息

Küçükçongar Yavaş Aynur, Orhaner Betül, Genç Pınar, Kılıç Nevin, Erdoğan Hakan, Özdemir Özlem, Ekici Arzu

机构信息

Şevket Yılmaz Training and Research Hospital, Clinic of Pediatric Metabolism, Bursa, Turkey.

出版信息

Turk J Haematol. 2017 Aug 2;34(3):264-265. doi: 10.4274/tjh.2015.0454. Epub 2016 Apr 18.

DOI:10.4274/tjh.2015.0454

PMID:27094156

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5544048/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18a1/5544048/99d5bdaf9b6a/TJH-34-264-g1.jpg

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Expression of lysosomal acid lipase mutants detected in three patients with cholesteryl ester storage disease.

Hum Mol Genet. 1996 Oct;5(10):1611-7. doi: 10.1093/hmg/5.10.1611.

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Secondary Hemophagocytic Lymphohistiocytosis in an Infant with Wolman Disease.

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