How to handle HMG-CoA lyase deficiency and type 1 diabetes? A challenging case report-Reference-Cited by-同舟云学术

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How to handle HMG-CoA lyase deficiency and type 1 diabetes? A challenging case report

Published:2023-11 Issue:9 Volume:70 Page:609-611
ISSN:2530-0180
Container-title:Endocrinología, Diabetes y Nutrición (English ed.)
language:en
Short-container-title:Endocrinología, Diabetes y Nutrición (English ed.)

Author:

Morais André,Pinheiro Teresa,Figueiredo Ana Sofia,Correia Cíntia Castro,Campos Teresa,Rodrigues Esmeralda,Teles Elisa Leão

Publisher

Elsevier BV

Subject

Nutrition and Dietetics,Endocrinology,Endocrinology, Diabetes and Metabolism

Reference12 articles.

1. A newborn screening approach to diagnose 3-hydroxy-3-methylglutaryl-CoA lyase deficiency;Václavík;JIMD Rep,2020

2. Molecular genetics of HMG-CoA lyase deficiency;Pié;Mol Genet Metab,2007

3. 3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: one disease – many faces;Grünert;Orphanet J Rare Dis,2020

4. 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency: a case report and literature review;Yilmaz;Nutr Hosp,2018

5. Type 1 diabetes in children and adolescents: a position statement by the American Diabetes Association;Chiang;Diabetes Care,2018

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