نتایج جستجو برای: congenital adrenal hyperplasia cah

تعداد نتایج: 200998  

2012
Hooman Angoorani Zohreh Haratian Farzin Halabchi

BACKGROUND Congenital Adrenal Hyperplasia (CAH) refers to a group of congenital conditions characterized by disordered cortisol synthesis. The correlation between CAH and sports performance has been less studied before and there is very limited information regarding the impacts of this congenital disease on sports performance. Probably, there are some limitations for patients who suffer from CA...

Journal: :Arquivos brasileiros de endocrinologia e metabologia 2014
Sara Reis Teixeira Paula Condé Lamparelli Elias Marco Túlio Soares Andrade Andrea Farias Melo Jorge Elias Junior

Congenital adrenal hyperplasia (CAH) is an autossomic recessive disorder caused by impaired steroidogenesis. Patients with CAH may present adrenal insufficiency with or without salt-wasting, as well as various degrees of virilization and fertility impairment, carrying a high incidence of testicular adrenal rest tumors and increased incidence of adrenal tumors. The diagnosis of CAH is made based...

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 ...

2017
Carla Bizzarri Elisa Pisaneschi Mafalda Mucciolo Stefania Pedicelli Daniela Galeazzi Antonio Novelli Marco Cappa

BACKGROUND Lipoid congenital adrenal hyperplasia (CAH) (OMIM n. 201710) is the most severe form of congenital adrenal hyperplasia. It is characterized by severe adrenal and gonadal steroidogenesis impairment due to a defect in the conversion of cholesterol to pregnenolone. Affected infants experience salt loss, but glucocorticoid and mineralocorticoid replacement therapy enables long-term survi...

Journal: :Journal of pediatric endocrinology & metabolism : JPEM 2006
David E Reichman Perrin C White Maria I New Zev Rosenwaks

Congenital adrenal hyperplasia (CAH) is the most frequently encountered genetic steroid disorder affecting fertility. Steroid hormones play a crucial role in sexual development and reproductive function; patients with either 21- hydroxylase or 11β-hydroxylase deficiency thus face immense challenges to their fertility. Given the relevance of CAH in reproductive medicine as well as the diagnostic...

2012
Gül Bahtiyar Alan Sacerdote

The main aim of the chapter entitled Management Approaches to Congenital Adrenal Hyperplasia (CAH) in Adolescents and Adults; Latest Therapeutic Developments, will be first to familiarize readers with current treatment guidelines using glucocorticoid and mineralocorticoid replacement in treating this common and under-diagnosed cause of amenorrhea. Next, to introduce readers to the concept of in...

Journal: :The British journal of radiology 2015
H K Kok M Sherlock N A Healy O Doody P Govender W C Torreggiani

Congenital adrenal hyperplasia (CAH) is a genetic autosomal recessive condition most frequently as a result of a mutation in the 21-hydroxylase enzyme gene. Patients with poorly controlled CAH can manifest characteristic imaging findings as a result of adrenocorticotrophic hormone stimulation or the effects of cortisol precursor excess on various target organs. We present a spectrum of imaging ...

Journal: :medical journal of islamic republic of iran 0
firouzeh nili from the department of pediatrics, imam khomeini hospital, tehran university of medical sciences,

a four day old female infant was admitted because of poor feeding, vomiting and jaundice. laboratory examination showed hyperkalemia, mild hyponatremia and renal tubular acidosis type 4. serum aldosterone and plasma renin activity were elevated but serum cortisol, 17 -hydroxyprogesterone, acth, 24 hour urinary 17- ketoste roid, pregnanetriol, renal function and sonogram were normal and hence ps...

2015
Atsumi Tsuji Kaoru Konishi Satomi Hasegawa Akira Anazawa Toshikazu Onishi Makoto Ono Tomohiro Morio Teruo Kitagawa Kenichi Kashimada

BACKGROUND Congenital adrenal hyperplasia (CAH) cause life-threatening adrenal crisis. It also affects fetal sex development and can result in incorrect sex assignment at birth. In 1989, a newborn screening program for congenital adrenal hyperplasia (CAH) was introduced in Tokyo. Here we present the results of this screening program in order to clarify the efficiency of CAH screening and the in...

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