Familial glucocorticoid deficiency (Q101051): Difference between revisions
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Latest revision as of 17:50, 16 August 2026
Familial Glucocorticoid Deficiency (FGD) syndrome is a genetic adrenal insufficiency without mineralocorticoid deficiency presenting with recurrent hypoglycaemia (triggered, for example, by infectious episodes) that may lead to convulsions or even coma, chronic asthenia, frequent infections, susceptibility to allergies, and usually skin pigmentation.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_861297039 |
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| English | Familial glucocorticoid deficiency |
Familial Glucocorticoid Deficiency (FGD) syndrome is a genetic adrenal insufficiency without mineralocorticoid deficiency presenting with recurrent hypoglycaemia (triggered, for example, by infectious episodes) that may lead to convulsions or even coma, chronic asthenia, frequent infections, susceptibility to allergies, and usually skin pigmentation. |
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CID11:ID_861297039
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dki-india-ID_861297039
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Concluído
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15 August 2026
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