نتایج جستجو برای: hydroxylase deficiency

تعداد نتایج: 152075  

2011
Ricardo P. P. Moreira Alexander A. L. Jorge Larissa G. Gomes Laura C. Kaupert João Massud Filho Berenice B. Mendonca Tânia A. S. S. Bachega

INTRODUCTION 21-hydroxylase deficiency is an autosomal recessive disorder that causes glucocorticoid deficiency and increased androgen production. Treatment is based on glucocorticoid replacement; however, interindividual variability in the glucocorticoid dose required to achieve adequate hormonal control has been observed. OBJECTIVE The present study aimed to evaluate the association between...

Journal: :Clinical chemistry 1997
J Oriola I Plensa I Machuca C Pavía F Rivera-Fillat

Impaired synthesis of adrenal steroid hormones because of steroid 21-hydroxylase deficiency is one of the most common inborn errors of metabolism. To expedite molecular diagnosis in families with 21-hydroxylase deficiency, we have designed a rapid strategy to determine nine of the most common mutations in the 21-hydroxylase gene. According to the mutation to be detected, we apply either of two ...

Journal: :Proceedings of the National Academy of Sciences 1999

Journal: :Annals of Clinical Biochemistry: International Journal of Laboratory Medicine 1977

2017
Daniel Powell Taiga Inoue Gül Bahtiyar Gabriel Fenteany Alan Sacerdote

An elderly woman presented with acne and male pattern alopecia, which upon diagnostic evaluation was found to be due to nonclassic 11-hydroxylase deficiency. We previously reported that Ashwagandha root ameliorates nonclassic 3-β-ol dehydrogenase and aldosterone synthase deficiencies. This is the first report of its use being associated with amelioration of nonclassic 11-hydroxylase deficiency,...

2015
Tomohiro Ishii Makoto Anzo Masanori Adachi Kazumichi Onigata Satoshi Kusuda Keisuke Nagasaki Shohei Harada Reiko Horikawa Masanori Minagawa Kanshi Minamitani Haruo Mizuno Yuji Yamakami Masaru Fukushi Toshihiro Tajima

Purpose of developing the guidelines: The first guidelines for diagnosis and treatment of 21-hydroxylase deficiency (21-OHD) were published as a diagnostic handbook in Japan in 1989, with a focus on patients with severe disease. The "Guidelines for Treatment of Congenital Adrenal Hyperplasia (21-Hydroxylase Deficiency) Found in Neonatal Mass Screening (1999 revision)" published in 1999 were rev...

Journal: :Archives of disease in childhood 2002
E Charmandari C G D Brook P C Hindmarsh

Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is an autosomal recessive condition in which deletions or mutations of the cytochrome P450 21-hydroxylase gene cause glucocorticoid and often mineralocorticoid deficiency. Despite optimal substitution therapy, control of classical CAH is often inadequate at puberty, and the problems encountered relate to hypocortisolism and/o...

Phenylketonuria (PKU) is the most common autosomal recessive disorder of amino acid metabolism. Thedisease is caused mainly by mutations in the phenylalanine hydroxylase (PAH) gene, encoding phenylalaninehydroxylase (PAH) enzyme. The PAH enzyme deficiency results in the elevation of phenylalanine inthe blood, which may cause severe irreversible mental retardation in the affect...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید