eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | congenital adrenal hyperplasia |
| Symptom | C1384514|primary aldosteronism |
| Sentences | 4 |
| PubMedID- 22308486 | These findings demonstrate striking variations in phenotypes and clinical outcome resulting from different mutations of the same amino acid in kcnj5 and have implications for the diagnosis and pathogenesis of primary aldosteronism with and without adrenal hyperplasia. |
| PubMedID- 21297325 | The clinical diagnosis of subclinical cushing's syndrome due to acth-independent macronodular adrenal hyperplasia (aimah) associated with primary aldosteronism was made, and he underwent left adrenalectomy; the resected adrenal lesion was consistent with the pathological diagnosis of aimah coexistent with aldosterone-producing adenoma (apa). |
| PubMedID- 24133375 | These observations warrant additional studies in low renin hypertension, preferably in comparison with patients matched for age, gender, and blood pressure, and having primary aldosteronism due to bilateral adrenal hyperplasia, which is the commonest cause of autonomous aldosterone secretion. |
| PubMedID- 23087856 | These are two other forms of primary aldosteronism associated with adrenal hyperplasia: familial hyperaldosteronism type i and type ii figure 1. |
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