Amaç: Geç başlangıçlı konjenital hiperplazi (NK-KAH) tanısında 1 mg IM sentetik ACTH depo preparatın, altın standart test olarak kabul edilen 0,25 mg IV sentetik ACTH ile karşılaştırılması. Materyal-Metod: Ege üniversitesi tıp fakültesi endokrinoloji bilim dalı polikliniğine hirsutizm şikayeti ile başvuran ve folliküler evre 17-OHP değerleri 2 ng/ml'nin üzerinde olan 50 bayana (yaş ortalaması: 25,1±1,9) birbirini izleyen adet dönemlerinde 0,25 mg IV ve 1 mg IM synacthen uyarı testleri yapıldı. Bazal, 30. ,60. 90. ve 120. dakikalarda 17-OHP, androstenedion ve 11 deoksikortizol değerleri ölçülde. Tüm hastaların erken folliküler evre hormon ve klinink parametreleri değerlendirildi. 0,25 mg IV test ile 1 mg IM testin sonuçları karşılaştırıldı. ...
Congenital adrenal hyperplasia (CAH) is a group of disorders with autosomal recessive inheritance an...
BACKGROUND: Congenital adrenal hyperplasia is a group of disorders caused by defects in the adrenal ...
A modified short ACTH test for the detection of heterozygote carriers of 21-hydroxylse deficiency (2...
OBJETIVOS: avaliar se os níveis de 17-hidroxiprogesterona podem predizer o resultado do teste de est...
Newborn screening for congenital adrenal hyperplasia (CAH) has high false-positive rates, necessitat...
Non-classic congenital adrenal hyperplasia (NCAH) is a rare cause of hirsutism and it results from a...
P>Background Congenital adrenal hyperplasia caused by classic 21-hydroxylase deficiency (21OHD) is a...
SUMMARY. A robust assay for routine measurement of blood-spot 17a-hydroxyprogesterone (17-0HP) conce...
Heterozygote carriers of 21-hydroxylase deficiency (21-OHD) cannot be detected by measurements of ba...
OBJECTIVE: The short synacthen test (SST) is widely used to assess patients for adrenal insufficienc...
CAHスクリーニング方法を改良する目的で,改良型抗体を用いる試薬であるエンザプレートNeo-17α-OHPについて,基礎的検討および従来型試薬であるN-17α-OHPや高感度HPLC法との比較等を行い...
Synacthen test has been widely used as a screening test for evaluation of adrenal cortisol reserve. ...
OBJECTIVE: Newborn screening based on measurement of 17alpha-hydroxyprogesterone (17-OHP) in a dried...
A forma não-clássica da hiperplasia adrenal congênita (HAC) por deficiência da 21-hidroxilase (D21OH...
Background: Undiagnosed congenital adrenal hyperplasia (CAH) can cause adrenal incidentalomas, but t...
Congenital adrenal hyperplasia (CAH) is a group of disorders with autosomal recessive inheritance an...
BACKGROUND: Congenital adrenal hyperplasia is a group of disorders caused by defects in the adrenal ...
A modified short ACTH test for the detection of heterozygote carriers of 21-hydroxylse deficiency (2...
OBJETIVOS: avaliar se os níveis de 17-hidroxiprogesterona podem predizer o resultado do teste de est...
Newborn screening for congenital adrenal hyperplasia (CAH) has high false-positive rates, necessitat...
Non-classic congenital adrenal hyperplasia (NCAH) is a rare cause of hirsutism and it results from a...
P>Background Congenital adrenal hyperplasia caused by classic 21-hydroxylase deficiency (21OHD) is a...
SUMMARY. A robust assay for routine measurement of blood-spot 17a-hydroxyprogesterone (17-0HP) conce...
Heterozygote carriers of 21-hydroxylase deficiency (21-OHD) cannot be detected by measurements of ba...
OBJECTIVE: The short synacthen test (SST) is widely used to assess patients for adrenal insufficienc...
CAHスクリーニング方法を改良する目的で,改良型抗体を用いる試薬であるエンザプレートNeo-17α-OHPについて,基礎的検討および従来型試薬であるN-17α-OHPや高感度HPLC法との比較等を行い...
Synacthen test has been widely used as a screening test for evaluation of adrenal cortisol reserve. ...
OBJECTIVE: Newborn screening based on measurement of 17alpha-hydroxyprogesterone (17-OHP) in a dried...
A forma não-clássica da hiperplasia adrenal congênita (HAC) por deficiência da 21-hidroxilase (D21OH...
Background: Undiagnosed congenital adrenal hyperplasia (CAH) can cause adrenal incidentalomas, but t...
Congenital adrenal hyperplasia (CAH) is a group of disorders with autosomal recessive inheritance an...
BACKGROUND: Congenital adrenal hyperplasia is a group of disorders caused by defects in the adrenal ...
A modified short ACTH test for the detection of heterozygote carriers of 21-hydroxylse deficiency (2...