A newborn with glycogen storage disease type Ib presenting with hypoglycemia and evidence of mitochondrial dysfunction

Glycogen storage disease type Ib (GSDIb) is an inherited disorder of carbohydrate metabolism that commonly presents in infancy. Here, we describe a case of GSDIb who presented on the first day of life with severe hypoglycemia and lactic acidosis, prompting a broad differential diagnosis. Additional testing revealed hyperlipidemia, relatively low ketones, and elevations of TCA-cycle intermediates in urine suggestive of primary or secondary mitochondrial dysfunction. The diagnosis of GSDIb was established by genome sequencing showing homozygous likely pathogenic variants in SLC37A4 . This case highlights the importance of including GSDIb in the differential diagnosis of neonatal hypoglycemia and reinforces the underreported metabolic pattern of mitochondrial dysfunction that can be seen in GSDIb.

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Publication Details

Journal
Molecular Genetics and Metabolism Reports
Published
2026-09-24
DOI
https://doi.org/10.1016/j.ymgmr.2026.101364
Primary Topic
Glycogen Storage Diseases and Myoclonus
Type
article
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article

A newborn with glycogen storage disease type Ib presenting with hypoglycemia and evidence of mitochondrial dysfunction

Tina M. Cowan, Meredith Fuchs, Gregory M. Enns, Laura Keehan et al.
Molecular Genetics and Metabolism Reports
Glycogen Storage Diseases and Myoclonus
article

A newborn with glycogen storage disease type Ib presenting with hypoglycemia and evidence of mitochondrial dysfunction

Tina M. Cowan, Meredith Fuchs, Gregory M. Enns, Laura Keehan, Tyler Ky
article en

Abstract

Glycogen storage disease type Ib (GSDIb) is an inherited disorder of carbohydrate metabolism that commonly presents in infancy. Here, we describe a case of GSDIb who presented on the first day of life with severe hypoglycemia and lactic acidosis, prompting a broad differential diagnosis. Additional testing revealed hyperlipidemia, relatively low ketones, and elevations of TCA-cycle intermediates in urine suggestive of primary or secondary mitochondrial dysfunction. The diagnosis of GSDIb was established by genome sequencing showing homozygous likely pathogenic variants in SLC37A4 . This case highlights the importance of including GSDIb in the differential diagnosis of neonatal hypoglycemia and reinforces the underreported metabolic pattern of mitochondrial dysfunction that can be seen in GSDIb.

Molecular Genetics and Metabolism ReportsVol. 49
Emory University (US), Stanford University (US)
Good health and well-being
Openalex Percentile: Top 10%
Glycogen Storage Diseases and Myoclonus
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