Novel PYGL mutations in Chinese children leading to glycogen storage disease type VI: two case reports.

Abstract

BACKGROUND:

PYGL mutations can cause liver phosphorylase deficiency, resulting in a glycogenolysis disorder, namely, glycogen storage disease (GSD) VI. The disease is rarely reported in the Chinese population. GSD VI is mainly characterized in untreated children by hepatomegaly, growth retardation and elevated liver transaminases.

CASE PRESENTATION:

In this study, we report two GSD VI patients with growth retardation and abnormal liver function. There was no obvious hepatomegaly for one of them. Whole exome sequencing (WES) combined with copy number variation analysis was performed. We found a novel homozygous gross deletion, c.1621-258_2178-23del, including exons 14-17 of PYGL in patient 1. The exons 14-17 deletion of PYGL resulted in an in-frame deletion of 186 amino acids. Compound heterozygous mutations of PYGL were identified in patient 2, including a novel missense mutation c.1832C > T/p.A611V and a recurrent nonsense mutation c.280C > T/p.R94X. After treatment with uncooked cornstarch (UCS) 8 months for patient 1 and 13 months for patient 2, the liver transaminases of both patients decreased to a normal range and their stature was improved. However, patient 1 still showed mild hypertriglyceridemia.

CONCLUSIONS:

We describe two GSD VI patients and expand the spectrum of PYGL mutations. Patient 1 in this study is the first GSD VI case that showed increased transaminases without obvious hepatomegaly due to a novel homozygous gross deletion of PYGL identified through WES.

• Authors: Xiaomei Luo, Jiacheng Hu, Xueren Gao, Yanjie Fan, Yu Sun, Xuefan Gu, Wenjuan Qiu
• Journal: BMC medical genetics (BMC Med Genet) Vol. 21 Issue 1 Pg. 74 (04 08 2020) ISSN: 1471-2350 [Electronic] England
• PMID: 32268899 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Glycogen Phosphorylase, Liver Form
• PYGL protein, human

Topics

• Child, Preschool
• China
• Female
• Glycogen Phosphorylase, Liver Form (genetics)
• Glycogen Storage Disease Type VI (complications, genetics, metabolism, pathology)
• Hepatomegaly (etiology, genetics)
• Humans
• Infant
• Liver (pathology)
• Mutation
• Polymorphism, Genetic
• Sequence Deletion