نتایج جستجو برای: adrenal hyperplasia

تعداد نتایج: 84522  

R VAKILI,

In this study the clinical and epidemiological characteristics of congenital adrenal hyperplasia were evaluated prospectively in 47 patients admitted in Imam Reza Hospital in Mashhad during a 4 year period. 21-hydroxylase deficiency was present in 42 patients (89.3%), the simple virilizing form in 6 and the salt-losing form in 36 of them. 11b hydroxylase deficiency was present in 5 patient...

2005
Esra Deniz Papatya Çakır Fatma Şentürk Mutlu Erdal Eren Aliye Özlem Paşa Halil Sağlam Ömer Tarım

Congenital adrenal hyperplasia refers to a group of autosomal recessive disorders caused by a deficiency of an enzyme involved in the synthesis of glucocorticoids. The enzyme deficiency generally leads to a deficiency of cortisol and/or aldosterone production within the adrenal cortex. The lack of glucocorticoids generally leads to elevated levels of plasma corticotropin (ACTH), which often res...

Journal: :Journal of tropical pediatrics 2011
N A Bausch-Becker H C Ribeiro M B Krawinkel

Neonatal screening for congenital adrenal hyperplasia: experience and results in Argentina. J Pediatr Endocrinol Metab 2008;21:73–8. 19. Cordova RA, Vignola G. Screening and diagnosis of congenital adrenal hyperplasia in Basilicata (Italy). Southeast Asian J Trop Med Pub Health 1999;30: 103–6. 20. Valentino R, Tommaselli AP, Rossi R, et al. A pilot study for neonatal screening of congenital adr...

Journal: :Dermato-Endocrinology 2009

Journal: :international journal of preventive medicine 0
mahin hashemipour mahmoud ghasemi silva hovsepian

lipoid congenital adrenal hyperplasia (lipoid cah), a rare disorder of steroid biosynthesis, is the most severe form of cah. in this disorder the synthesis of glucocorticoids, mineralocorticoids and sex steroids is impaired which result in adrenal failure, severe salt wasting crisis and hyperpigmentation in phenotypical female infants irrespective of genetic sex. in this report, we presented a ...

2015
Carlos Esteban Builes-Montaño Carlos Andrés Villa-Franco Alejandro Román-Gonzalez Alejandro Velez-Hoyos Santiago Echeverri-Isaza

The primary bilateral macronodular adrenal hyperplasia or the independent adrenocorticotropic hormone bilateral nodular adrenal hyperplasia is a rare cause hypercortisolism, its diagnosis is challenging and there is no clear way to decide the best therapeutic approach. Adrenal venous sampling is commonly used to distinguish the source of hormonal production in patients with primary hyperaldoste...

Journal: :Archives of Disease in Childhood 1951

Journal: :Endocrine journal 2004
Toshihiro Imaki Mitsuhide Naruse Kazue Takano

Diffuse or nodular hyperplasia of adrenal glands is associated frequently with ACTH-dependent Cushing's syndrome. We carried out a retrospective analysis of 28 patients with ACTH-dependent Cushing's syndrome admitted to our institution between 1984 and 1999 in order to clarify the incidence of adrenal hyperplasia in ACTH-dependent Cushing's syndrome and also to determine the correlation between...

Journal: :Endocrinology and Metabolism Clinics of North America 2015

Journal: :Polish journal of pathology : official journal of the Polish Society of Pathologists 2012
Anna Babinska Adam Nałecz Renata Swiatkowska-Stodulska Krzysztof Sworczak

Adrenal myelolipoma is a benign neoplasm composed of an admixture of hemopoietic elements and mature adipose tissue. The incidence of adrenal myelolipoma is reported as between 4% and 5% of adrenal incidentaloma. The association of an adrenal myelolipoma and adrenal nodular hyperplasia or adrenal adenoma is rare. Four cases of adrenal myelolipomas in the material of 702 incidentally discovered ...

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