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`Male pseudohermaphroditism with 17 alpha-hydroxylase deficiency. A case report. - PubMed - NCBI
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`PubMed
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`Format: Abstract
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`Br J Obstet Gynaecol. 1980 Dec;87(12):1162-5.
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`Male pseudohermaphroditism with 17 alpha-hydroxylase deficiency. A
`case report.
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`Abad L, Parrilla JJ, Marcos J, Gimeno F, López Bernal A.
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`Abstract
`A case of male pseudohermaphroditism with 17 alpha-hydroxylase deficiency is reported in a 23-
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`year-old woman presenting with primary amenorrhoea and a history of bilateral inguinal hernia
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`repair. She was tall, had hypoplastic external genitalia with a blood pressure of 220/140 mm Hg. Her
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`karyotype was XY. Acute adrenal failure occurred following exploratory laparotomy. After treatment
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`with glucocorticoids and oestrogens, the hormone and electrolyte profiles returned to normal and the
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`blood pressure fell. The biochemical implications of this enzyme deficiency are discussed.
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`PMID: 6254560
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`[PubMed - indexed for MEDLINE]
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