Transient infantile hypertriglyceridemia caused by GPD1 deficiency : report of two cases and literature review

Objective: To investigate the clinical phenotype and genotype of transient infantile hypertriglyceridemia (HTGTI). Methods: The clinical data of two HTGTI children, diagnosed at Children's Hospital of Fudan University from July 2019 to January 2020, were collected and analyzed retrospectively....

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Bibliographische Detailangaben

Veröffentlicht in:	Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 58(2020), 11 vom: 02. Nov., Seite 923-927
1. Verfasser:	Xie, X B (VerfasserIn)
Weitere Verfasser:	Li, M P, Wang, J S
Format:	Online-Aufsatz
Sprache:	Chinese
Veröffentlicht:	2020
Zugriff auf das übergeordnete Werk:	Zhonghua er ke za zhi = Chinese journal of pediatrics
Schlagworte:	Case Reports Journal Article Review Child Disease attributes Genes Hypertriglyceridemia Glycerophosphates Glycerolphosphate Dehydrogenase EC 1.1.-