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....
| Publié dans: | Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 58(2020), 11 vom: 02. Nov., Seite 923-927 |
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| Auteur principal: | |
| Autres auteurs: | , |
| Format: | Article en ligne |
| Langue: | Chinese |
| Publié: |
2020
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| 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.- |
| Accès en ligne |
Volltext |