Isolated glycerol kinase deficiency (Q98861): Difference between revisions
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Revision as of 15:30, 16 August 2026
This is an isolated X-linked recessive enzyme defect that is heterozygous in nature. Three clinically distinct forms of this deficiency have been proposed, namely infantile, juvenile, and adult.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_542432712 |
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| English | Isolated glycerol kinase deficiency |
This is an isolated X-linked recessive enzyme defect that is heterozygous in nature. Three clinically distinct forms of this deficiency have been proposed, namely infantile, juvenile, and adult. |
Statements
CID11:ID_542432712
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