MALE PSEUDOHERMAPHRODITISM WITH 17alpha-HYDROXYLASE DEFICIENCY. A CASE REPORT
Author:
Publisher
Wiley
Subject
Obstetrics and Gynaecology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1471-0528.1980.tb04491.x/fullpdf
Reference13 articles.
1. 17-hydroxylation deficiency in man.
2. A New Male Pseudohermaphroditism Associated with Hypertension due to a Block of 17α-Hydroxylation
3. Primäre Amenorrhoe und Hypokaliämie infolge 17alpha-Hydroxylase-Mangels
4. SEX HORMONE LEVELS AND GONADOTROPHIN RELEASE IN PREMATURE OVARIAN FAILURE
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1. An Asian case of combined 17α-hydroxylase/17,20-lyase deficiency due to homozygous p.R96Q mutation: A case report and review of the literature;Frontiers in Endocrinology;2022-10-19
2. P450c17 Deficiency Caused by Compound Heterozygosity for Two Novel Mutations Presenting as Hypotension in Early Infancy;Hormone Research in Paediatrics;2011
3. A Male Patient Presenting with Major Clinical Symptoms of Glucocorticoid Deficiency and Skeletal Dysplasia, showing a Steroid Pattern Compatible with 17.ALPHA.-Hydroxylase/ 17, 20-Lyase Deficiency, but without Obvious CYP 17 Gene Mutations.;Endocrine Journal;1999
4. Role of cytochrome P450c17 in polycystic ovary syndrome;Molecular and Cellular Endocrinology;1998-10
5. Long Term Follow-Up of a 46,XY Phenotypic Girl with 17.ALPHA.-Hydroxylase Deficiency Treated with Alternate-Day Dexamethasone.;Endocrine Journal;1998
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