Familial glucocorticoid deficiency (Q101051): Difference between revisions
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A síndrome da deficiência de glicocorticoide familiar é uma insuficiência adrenal genética sem deficiência de mineralocorticoide que se apresenta com hipoglicemia recorrente (desencadeada, por exemplo, por episódios infecciosos) que pode levar a convulsões ou mesmo coma, astenia crônica, infecções frequentes, suscetibilidade a alergias e, geralmente pigmentação da pele. | |||
| description / en | description / en | ||
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. | |||
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 |
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| 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. |
