Male pseudohermaphroditism due to 17-ketoreductase deficiency: Report of a case without gynecomastia and without vaginal pouch
A black adult subject, exhibiting complete virilization at puberty with psychological female orientation, was investigated. An older sister had similar physical habitus. Hormonal data showed an androstenedione/testosterone ratio > 1. This led us to the diagnosis of 17-ketoreductase deficiency, wi...
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| Veröffentlicht in: | American journal of obstetrics and gynecology 1986-01, Vol.154 (1), p.148-149 |
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| container_title | American journal of obstetrics and gynecology |
| container_volume | 154 |
| creator | Caufriez, Anne |
| description | A black adult subject, exhibiting complete virilization at puberty with psychological female orientation, was investigated. An older sister had similar physical habitus. Hormonal data showed an androstenedione/testosterone ratio > 1. This led us to the diagnosis of 17-ketoreductase deficiency, with possible genetic transmission of the defect. |
| doi_str_mv | 10.1016/0002-9378(86)90413-8 |
| format | Article |
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An older sister had similar physical habitus. Hormonal data showed an androstenedione/testosterone ratio > 1. This led us to the diagnosis of 17-ketoreductase deficiency, with possible genetic transmission of the defect.</description><identifier>ISSN: 0002-9378</identifier><identifier>EISSN: 1097-6868</identifier><identifier>DOI: 10.1016/0002-9378(86)90413-8</identifier><identifier>PMID: 3004217</identifier><identifier>CODEN: AJOGAH</identifier><language>eng</language><publisher>Philadelphia, PA: Elsevier Inc</publisher><subject>17-Hydroxysteroid Dehydrogenases - deficiency ; 17-ketoreductase deficiency ; Adrenocorticotropic Hormone ; Adult ; Biological and medical sciences ; Chorionic Gonadotropin ; Disorders of Sex Development - enzymology ; Disorders of Sex Development - genetics ; Disorders of Sex Development - surgery ; Female ; Gynecology. Andrology. Obstetrics ; Gynecomastia - pathology ; Hormones - blood ; Humans ; Male ; Male and female genital diseases. Gonadal dysgenesis. Hermaphroditism. 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An older sister had similar physical habitus. Hormonal data showed an androstenedione/testosterone ratio > 1. This led us to the diagnosis of 17-ketoreductase deficiency, with possible genetic transmission of the defect.</description><subject>17-Hydroxysteroid Dehydrogenases - deficiency</subject><subject>17-ketoreductase deficiency</subject><subject>Adrenocorticotropic Hormone</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Chorionic Gonadotropin</subject><subject>Disorders of Sex Development - enzymology</subject><subject>Disorders of Sex Development - genetics</subject><subject>Disorders of Sex Development - surgery</subject><subject>Female</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Gynecomastia - pathology</subject><subject>Hormones - blood</subject><subject>Humans</subject><subject>Male</subject><subject>Male and female genital diseases. Gonadal dysgenesis. Hermaphroditism. Sex hormones resistance</subject><subject>Male pseudohermaphroditism</subject><subject>Medical sciences</subject><subject>Vagina - abnormalities</subject><issn>0002-9378</issn><issn>1097-6868</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1986</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE2LFDEQhoMo67j6DxRyEFkPrUl3Okl7EGTxC1YE0XOoTio70e5Ob5LeZS7-dnt2hjl6Kor3eYviIeQ5Z2844_ItY6yuukbpCy1fd0zwptIPyIazTlVSS_2QbE7IY_Ik59_7te7qM3LWMCZqrjbk7zcYkM4ZFxe3mEaYtym6UEIeqVuQlki5qv5giQndYgtkpA59sAEnu3tHf-AcU6HRU6B2H96Fso1Lode7CW0cIZcAFCZ3Cm7hOkww0DkudvuUPPIwZHx2nOfk16ePPy-_VFffP3-9_HBV2UbLUqm-b2rwzEnVu7ZFb4WXyqPzPfQILQfRNVb0TFnROC1r6XUn2p4Jwb2UfXNOXh3uzineLJiLGUO2OAwwYVyyUVKt2up6BcUBtCnmnNCbOYUR0s5wZvbazV6i2Ts1Wpp77UavtRfH-0s_ojuVjp7X_OUxh2xh8AkmG_IJ06qVrexW7P0Bw9XFbcBk8r1odCGhLcbF8P8__gHcqqEs</recordid><startdate>198601</startdate><enddate>198601</enddate><creator>Caufriez, Anne</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>198601</creationdate><title>Male pseudohermaphroditism due to 17-ketoreductase deficiency: Report of a case without gynecomastia and without vaginal pouch</title><author>Caufriez, Anne</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c386t-7bb32af0d67bd55efc4f67fedfbabea51a493c4b07c43d8626f8945b0441f66b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1986</creationdate><topic>17-Hydroxysteroid Dehydrogenases - deficiency</topic><topic>17-ketoreductase deficiency</topic><topic>Adrenocorticotropic Hormone</topic><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Chorionic Gonadotropin</topic><topic>Disorders of Sex Development - enzymology</topic><topic>Disorders of Sex Development - genetics</topic><topic>Disorders of Sex Development - surgery</topic><topic>Female</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Gynecomastia - pathology</topic><topic>Hormones - blood</topic><topic>Humans</topic><topic>Male</topic><topic>Male and female genital diseases. Gonadal dysgenesis. Hermaphroditism. Sex hormones resistance</topic><topic>Male pseudohermaphroditism</topic><topic>Medical sciences</topic><topic>Vagina - abnormalities</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Caufriez, Anne</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of obstetrics and gynecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Caufriez, Anne</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Male pseudohermaphroditism due to 17-ketoreductase deficiency: Report of a case without gynecomastia and without vaginal pouch</atitle><jtitle>American journal of obstetrics and gynecology</jtitle><addtitle>Am J Obstet Gynecol</addtitle><date>1986-01</date><risdate>1986</risdate><volume>154</volume><issue>1</issue><spage>148</spage><epage>149</epage><pages>148-149</pages><issn>0002-9378</issn><eissn>1097-6868</eissn><coden>AJOGAH</coden><abstract>A black adult subject, exhibiting complete virilization at puberty with psychological female orientation, was investigated. 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| fulltext | fulltext |
| identifier | ISSN: 0002-9378 |
| ispartof | American journal of obstetrics and gynecology, 1986-01, Vol.154 (1), p.148-149 |
| issn | 0002-9378 1097-6868 |
| language | eng |
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| source | MEDLINE; Elsevier ScienceDirect Journals Complete |
| subjects | 17-Hydroxysteroid Dehydrogenases - deficiency 17-ketoreductase deficiency Adrenocorticotropic Hormone Adult Biological and medical sciences Chorionic Gonadotropin Disorders of Sex Development - enzymology Disorders of Sex Development - genetics Disorders of Sex Development - surgery Female Gynecology. Andrology. Obstetrics Gynecomastia - pathology Hormones - blood Humans Male Male and female genital diseases. Gonadal dysgenesis. Hermaphroditism. Sex hormones resistance Male pseudohermaphroditism Medical sciences Vagina - abnormalities |
| title | Male pseudohermaphroditism due to 17-ketoreductase deficiency: Report of a case without gynecomastia and without vaginal pouch |
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