Mechanisms establishing the mineralocorticoid hormone patterns in the 17α-hydroxylase deficiency syndrome
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Biochemistry
Reference19 articles.
1. The characteristics, course and implications of the 17-hydroxylation deficiency in man;Biglieri,1973
2. Primäre Amenorrhoe und Hypokaliämie infolge 17alpha-Hydroxylase-Mangels;deLange;Dtsche Med. Wochenschr.,1977
3. A new male pseudohermaphroditism associated with hypertension due to a block of 17α-hydroxylation;Bricaire;J. clin. Endocr. Metab.,1972
4. 17-Hydroxylation deficiency in man;Biglieri;J. clin. Invest.,1966
5. Congenital adrenal hyperplasia secondary to 17-hydroxylase deficiency. Two sisters with amenorrhea, hypokalemia, hypertension, and cystic ovaries;Mallin;Ann. Intern. Med.,1969
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1. Atypical presentation in patients with 17 α-hydroxylase deficiency caused by a deletion in the cyp17a1 gene: short stature;The Turkish Journal of Pediatrics;2020
2. Functional Identification of Compound Heterozygous Mutations in the CYP17A1 Gene Resulting in Combined 17α-Hydroxylase/17,20-Lyase Deficiency;Endocrinology and Metabolism;2018
3. A late 17α-hydroxylase deficiency diagnosis that leads to the discovery of a new CYP17 gene mutation;Annales d'Endocrinologie;2015-02
4. A rare cause of hypertension in a healthy 2-year-old female: Questions;Pediatric Nephrology;2012-04-26
5. A rare cause of hypertension in a healthy 2-year-old female: Answers;Pediatric Nephrology;2012-04-26
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