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Adult glycerol kinase deficiency (GKD) is an uncommon form of GKD diagnosed fortuitously and characterized by pseudohypertriglyceridemia in otherwise healthy adults.
No clinical trials have been registered for glycerol kinase deficiency, adult form.
4 publications have been identified in PubMed for glycerol kinase deficiency, adult form. Research spans Case Report / Case Series (50%), Other (25%), and Review / Meta-Analysis (25%).
Madiraju SRM (2026). [PMID: 40927981](https://pubmed.ncbi.nlm.nih.gov/40927981/). *Endocr Rev*. [Review / Meta-Analysis]
Bregvadze K (2025). [PMID: 40171039](https://pubmed.ncbi.nlm.nih.gov/40171039/). *Clin Med Insights Endocrinol Diabetes*. [Case Report / Case Series]
Brothwell SL (2025). [PMID: 40068898](https://pubmed.ncbi.nlm.nih.gov/40068898/). *Arch Dis Child*. [Other]
Seferi S (2024). [PMID: 39473663](https://pubmed.ncbi.nlm.nih.gov/39473663/). *Cureus*. [Case Report / Case Series]
Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 5:40 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center