Glycogen storage diseases with liver involvement: a literature review of GSD type 0, IV, VI, IX and XI
Abstract Background Glycogen storage diseases (GSDs) with liver involvement are classified into types 0, I, III, IV, VI, IX and XI, depending on the affected enzyme. Hypoglycemia and hepatomegaly are hallmarks of disease, but muscular and renal tubular involvement, dyslipidemia and osteopenia can de...
Main Authors: | Miriam Massese, Francesco Tagliaferri, Carlo Dionisi-Vici, Arianna Maiorana |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2022-06-01
|
Series: | Orphanet Journal of Rare Diseases |
Subjects: | |
Online Access: | https://doi.org/10.1186/s13023-022-02387-6 |
Similar Items
-
Hepatic glycogen storage diseases type 0, VI and IX: description of an italian cohort
by: Francesco Tagliaferri, et al.
Published: (2022-07-01) -
Current understanding on pathogenesis and effective treatment of glycogen storage disease type Ib with empagliflozin: new insights coming from diabetes for its potential implications in other metabolic disorders
by: Arianna Maiorana, et al.
Published: (2023-04-01) -
Glycogen storage disease in two sisters: A case report
by: Sajal Twanabasu, et al.
Published: (2023-05-01) -
Hepatic glycogen synthase (GYS2) deficiency: seven novel patients and seven novel variants
by: Elena A. Kamenets, et al.
Published: (2020-05-01) -
Severe perioperative lactic acidosis in a pediatric patient with glycogen storage disease type Ia: a case report
by: Tamayo Takahashi, et al.
Published: (2023-12-01)