4.5 Article

Clinical and genetic spectrum of GSD type 6 in Korea

Journal

ORPHANET JOURNAL OF RARE DISEASES
Volume 18, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s13023-023-02750-1

Keywords

Glycogen storage disease; Molecular diagnosis; PYGL; Next-generation sequencing

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This study examined the clinical features, genetic analyses, and long-term outcomes of patients with GSD VI in Korea. Five patients were included in the study, and all patients showed symptoms such as hepatomegaly, elevated liver transaminase activity, and hypertriglyceridemia. Treatment with a high-protein diet and corn starch improved the liver function, hypertriglyceridemia, and height z score of the patients.
BackgroundGlycogen storage disease type VI (GSD VI) is a rare disease in which liver glycogen metabolism is impaired by mutations in the glycogen phosphorylase L (PYGL). This study aimed to examine the clinical features, genetic analyses, and long-term outcomes of patients with GSD VI in Korea.MethodsFrom January 2002 to November 2022, we retrospectively reviewed patients diagnosed with GSD VI using a gene panel at Seoul National University Hospital. We investigated the clinical profile, liver histology, molecular diagnosis, and long-term outcomes of patients with GSD VI.ResultsFive patients were included in the study. The age at onset was 18-30 months (median, 21 months), and current age was 3.7-17 years (median, 11 years). All patients showed hepatomegaly, elevated liver transaminase activity, and hypertriglyceridaemia. Hypercholesterolaemia and fasting hypoglycaemia occurred in 60% and 40% of patients, respectively. Ten variants of PYGL were identified, of which six were novel: five missense (p.[Gly607Val], p.[Leu445Pro], p.[Gly695Glu], p.[Val828Gly], p.[Tyr158His]), and one frameshift (p.[Arg67AlafsTer34]). All patients were treated with a high-protein diet, and four also received corn starch. All patients showed improved liver function tests, hypertriglyceridaemia, hepatomegaly, and height z score.ConclusionsThe GSD gene panel is a useful diagnostic tool for confirming the presence of GSD VI. Genetic heterogeneity was observed in all patients with GSD VI. Increased liver enzyme levels, hypertriglyceridaemia, and height z score in patients with GSD VI improved during long-term follow-up.

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