The evaluation of inherited metabolic diseases presenting with rhabdomyolysis from Turkey: Single center experience
Aim: It was aimed to identify markers that would indicate which cases presenting with rhabdomyolysis are more likely to be associated with inherited metabolic diseases. Methods: We analyzed 327 children who applied to our Hospital Pediatric Nutrition and Metabolic Diseases Clinic with rhabdomyolysis...
Main Authors: | Huseyin Bilgin, Ayse Ergul Bozaci |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2024-06-01
|
Series: | Molecular Genetics and Metabolism Reports |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2214426924000235 |
Similar Items
-
Glutaric aciduria and L-2-hydroxyglutaric aciduria: Clinical and molecular findings of 35 patients from Turkey
by: Ayse Ergül Bozaci, et al.
Published: (2023-09-01) -
An unexpected and devastating adverse event of dasatinib: Rhabdomyolysis
by: Burak Uz, et al.
Published: (2016-01-01) -
Case Report: Hemophagocytic Lymphocytosis in a Patient With Glutaric Aciduria Type IIC
by: Lingtong Huang, et al.
Published: (2022-01-01) -
Compilation of Genotype and Phenotype Data in <i>GCDH</i>-LOVD for Variant Classification and Further Application
by: Alexandra Tibelius, et al.
Published: (2023-12-01) -
Characterization and structure of the human lysine-2-oxoglutarate reductase domain, a novel therapeutic target for treatment of glutaric aciduria type 1
by: João Leandro, et al.
Published: (2022-09-01)