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....

Description complète

Détails bibliographiques
Publié dans:Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 58(2020), 11 vom: 02. Nov., Seite 923-927
Auteur principal: Xie, X B (Auteur)
Autres auteurs: Li, M P, Wang, J S
Format: Article en ligne
Langue:Chinese
Publié: 2020
Accès à la collection:Zhonghua er ke za zhi = Chinese journal of pediatrics
Sujets:Case Reports Journal Article Review Child Disease attributes Genes Hypertriglyceridemia Glycerophosphates Glycerolphosphate Dehydrogenase EC 1.1.-