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They were interviewed, and subsequently underwent laboratory evaluation for the detection of hypocortisolism.
2
In chronic hypocortisolism, adaptive changes in GR status seem to occur at the level of GR number.
3
The occurrence of hypocortisolism was higher among participants who had been on ART for a longer period of time.
4
The case we report had obesity, hypocortisolism but lacked red hair which is typical for subjects with POMC mutations.
5
In the course of steroid replacement therapy for hypocortisolism, the patient's arthralgia diminished, and MRI revealed shrinkage of the mass.
1
Adrenoleukodystrophy is a disorder of long-chain fatty acid metabolism associated with adrenalcorticalinsufficiency and central nervous system demyelination.
1
Clinical features and laboratory parameters were suggestive of underlying adrenocorticalinsufficiency.
2
There were no cases of acute adrenocorticalinsufficiency in the 274 patients who did not receive steroid replacement.
3
An endocrine evaluation (in absence of therapy) demonstrated panhypopituitarism with secondary hypothyroidism and adrenocorticalinsufficiency in presence of empty sella.
4
Four (7%) of the 57 patients receiving steroid replacement had episodes of acute adrenocorticalinsufficiency following operation and required increased steroid supplementation.
1
Background: Central adrenalinsufficiency is observed after cranial radiation therapy for cancer.
2
If adrenalinsufficiency should exist, it could considerably compromise postoperative recovery.
3
The converse of adrenalinsufficiency, that of adrenal excess, also exists.
4
The child was born prematurely with complete sex reversal and severe adrenalinsufficiency.
5
Conclusions: Relative adrenalinsufficiency occurs in a high proportion of patients with severe CAP.