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17α‐Hydroxylase deficiency in a genetic male and female sibling pair
Author(s) -
Sills Irene N.,
MacGillivray Margaret H.,
Amrhein James A.,
Migeon Claude J.,
Peterson Ralph E.
Publication year - 1981
Publication title -
international journal of gynecology and obstetrics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.895
H-Index - 97
eISSN - 1879-3479
pISSN - 0020-7292
DOI - 10.1016/0020-7292(81)90007-2
Subject(s) - medicine , congenital adrenal hyperplasia , cyp17a1 , sibling , endocrinology , 21 hydroxylase , secondary sex characteristic , corticosterone , amenorrhea , primary amenorrhea , pregnancy , genetics , hormone , biology , gene , psychology , developmental psychology
The diagnosis of congenital adrenal hyperplasia due to a deficiency of the enzyme 17α‐hydroxylase was made in a genetic male and female sibling pair born of parents who were first cousins. The genetic male was a phenotypic female who presented with primary amenorrhea and mild hypertension. The genetic female exhibited absence of secondary sexual characteristics and severe hypertension. The plasma steroid data confirmed the diagnosis of 17α‐hydroxylase deficiency in both subjects: low 17α‐hydroxyprogesterone, elevated desoxycorticosterone, elevated corticosterone and elevated progesterone. These are the first case reports of 17α‐hydroxylase deficiency in a male‐female sibling pair, and they add support to the hypothesis that this is an autosomal recessive disorder.