نتایج جستجو برای: adrenal hyperplasia

تعداد نتایج: 84522  

Journal: :Archives of Disease in Childhood 1971

Journal: :Journal of Clinical Investigation 1959

Journal: :The Journal of clinical endocrinology and metabolism 1999
N N'Diaye P Hamet J Tremblay J M Boutin L Gaboury A Lacroix

Gastric inhibitory polypeptide (GIP)-dependent Cushing's syndrome has been reported to occur either in unilateral adrenal adenoma or in bilateral macronodular adrenal hyperplasia. A 33-yr-old woman with Cushing's syndrome was found to have two 2.5- to 3-cm nodules in the right adrenal on computed tomography scan; the left adrenal appeared normal except for the presence of a small 0.8 x 0.6-cm n...

Journal: :International journal of advanced research 2022

Non-classical congenital adrenal hyperplasia by 21 hydroxylase deficiency is an autosomal recessive disease whose usual presentation a late virilization. In some African countries like Morocco, there are cultural barriers to gynecological examination in girls, women consult until for sexual problem as the case of our patient who consulted clitoris hypertrophy at age 22 years and hormonal assess...

Journal: :The Journal of clinical investigation 1943
N B Talbot A M Butler E A Maclachlan

The evidence of the literature indicates that the adrenal cortex produces a variety of hormones, some of which, like desoxycorticosterone, act predominantly to maintain a normal water and electrolyte balance (1), while others, like corticosterone, are effective chiefly through preventing hypoglycemia, either by facilitating the formation of sugar from protein (gluconeogenesis) (2) or by inhibit...

2015
Su Jin Lee Je Eun Song Sena Hwang Ji-Yeon Lee Hye-Sun Park Seunghee Han Yumie Rhee

Congenital adrenal hyperplasia (CAH) with 17α-hydroxylase/17,20-lyase deficiency is usually characterized by hypertension and primary amenorrhea, sexual infantilism in women, and pseudohermaphroditism in men. hypertension, and sexual infantilism in women and pseudohermaphroditism in men. In rare cases, a huge adrenal gland tumor can present as a clinical manifestation in untreated CAH. Adrenal ...

2016
Nilesh Lomte Tushar Bandgar Shruti Khare Swati Jadhav Anurag Lila Manjunath Goroshi Rajeev Kasaliwal Kranti Khadilkar Nalini S Shah

BACKGROUND Bilateral adrenal masses may have aetiologies like hyperplasia and infiltrative lesions, besides tumours. Hyperplastic and infiltrative lesions may have coexisting hypocortisolism. Bilateral tumours are likely to have hereditary/syndromic associations. The data on clinical profile of bilateral adrenal masses are limited. AIMS To analyse clinical, biochemical and radiological featur...

Journal: :Best practice & research. Clinical endocrinology & metabolism 2009
André Lacroix

Adrenocorticotropic hormone- (ACTH-)independent macronodular adrenal hyperplasia (AIMAH) is an infrequent cause of Cushing's syndrome (CS). AIMAH presents as incidental radiological finding or with subclinical or overt CS, occasionally with secretion of mineralocorticoids or sex steroids. The pathophysiology of this entity is heterogeneous. The aberrant adrenal expression and function of one or...

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