Loading…

Ovarian development in 46,XY gonadal dysgenesis

In humans the XY ovary is degenerative, there being scant evidence of persistence of that organ beyond the perinatal period. Here we describe indications of functional ovarian tissue in a 17-year-old female with male karyotype, H-Y+ cellular phenotype, and some signs of the Turner syndrome. Her gona...

Full description

Saved in:
Bibliographic Details
Published in:Human genetics 1982-01, Vol.60 (2), p.196-199
Main Authors: Russell, M H, Wachtel, S S, Davis, B W, Cahill, L T, Groos, E, Niblack, G D, Burr, I M
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c282t-1a4ca850d0042481a5701183ee652d81fa09ab1c7da422b1355b4c7ac6cd61723
cites cdi_FETCH-LOGICAL-c282t-1a4ca850d0042481a5701183ee652d81fa09ab1c7da422b1355b4c7ac6cd61723
container_end_page 199
container_issue 2
container_start_page 196
container_title Human genetics
container_volume 60
creator Russell, M H
Wachtel, S S
Davis, B W
Cahill, L T
Groos, E
Niblack, G D
Burr, I M
description In humans the XY ovary is degenerative, there being scant evidence of persistence of that organ beyond the perinatal period. Here we describe indications of functional ovarian tissue in a 17-year-old female with male karyotype, H-Y+ cellular phenotype, and some signs of the Turner syndrome. Her gonads were removed after the onset of secondary amenorrhea. Histological examination revealed a degenerative right ovary devoid of germ cells and follicles, and a left streak gonad. There was no trace of testicular development in either side.
doi_str_mv 10.1007/BF00569712
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_74039965</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>74039965</sourcerecordid><originalsourceid>FETCH-LOGICAL-c282t-1a4ca850d0042481a5701183ee652d81fa09ab1c7da422b1355b4c7ac6cd61723</originalsourceid><addsrcrecordid>eNpF0D1LA0EUheFBlBijjb2wlYW45t753C01GBUCaRS0Wu7O3MjKfsSdJJB_byRBq9M8nOIV4hLhDgHc-GEKYGzuUB6JIWolU5SgjsUQlIbUOnSn4izGLwA0uTQDMXDgrLQ4FOP5hvqK2iTwhutu2XC7Sqo20fb2_SP57FoKVCdhGz-55VjFc3GyoDryxWFH4m36-Dp5Tmfzp5fJ_Sz1MpOrFEl7ygwEAC11hmQcIGaK2RoZMlwQ5FSid4G0lCUqY0rtHXnrg0Un1Uhc73-Xffe95rgqmip6rmtquVvHwmlQeW7NDt7soe-7GHteFMu-aqjfFgjFb53iv84OXx1e12XD4Y8ecqgfQYZcbg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>74039965</pqid></control><display><type>article</type><title>Ovarian development in 46,XY gonadal dysgenesis</title><source>SpringerLink_过刊(NSTL购买)</source><creator>Russell, M H ; Wachtel, S S ; Davis, B W ; Cahill, L T ; Groos, E ; Niblack, G D ; Burr, I M</creator><creatorcontrib>Russell, M H ; Wachtel, S S ; Davis, B W ; Cahill, L T ; Groos, E ; Niblack, G D ; Burr, I M</creatorcontrib><description>In humans the XY ovary is degenerative, there being scant evidence of persistence of that organ beyond the perinatal period. Here we describe indications of functional ovarian tissue in a 17-year-old female with male karyotype, H-Y+ cellular phenotype, and some signs of the Turner syndrome. Her gonads were removed after the onset of secondary amenorrhea. Histological examination revealed a degenerative right ovary devoid of germ cells and follicles, and a left streak gonad. There was no trace of testicular development in either side.</description><identifier>ISSN: 0340-6717</identifier><identifier>EISSN: 1432-1203</identifier><identifier>DOI: 10.1007/BF00569712</identifier><identifier>PMID: 7076261</identifier><language>eng</language><publisher>Germany</publisher><subject>Adolescent ; Female ; Gonadal Dysgenesis - pathology ; Gonadal Dysgenesis, 46,XY - genetics ; Gonadal Dysgenesis, 46,XY - pathology ; H-Y Antigen - analysis ; HLA Antigens - analysis ; Humans ; Lymphocytes - analysis ; Ovary - pathology ; Phenotype</subject><ispartof>Human genetics, 1982-01, Vol.60 (2), p.196-199</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c282t-1a4ca850d0042481a5701183ee652d81fa09ab1c7da422b1355b4c7ac6cd61723</citedby><cites>FETCH-LOGICAL-c282t-1a4ca850d0042481a5701183ee652d81fa09ab1c7da422b1355b4c7ac6cd61723</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7076261$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Russell, M H</creatorcontrib><creatorcontrib>Wachtel, S S</creatorcontrib><creatorcontrib>Davis, B W</creatorcontrib><creatorcontrib>Cahill, L T</creatorcontrib><creatorcontrib>Groos, E</creatorcontrib><creatorcontrib>Niblack, G D</creatorcontrib><creatorcontrib>Burr, I M</creatorcontrib><title>Ovarian development in 46,XY gonadal dysgenesis</title><title>Human genetics</title><addtitle>Hum Genet</addtitle><description>In humans the XY ovary is degenerative, there being scant evidence of persistence of that organ beyond the perinatal period. Here we describe indications of functional ovarian tissue in a 17-year-old female with male karyotype, H-Y+ cellular phenotype, and some signs of the Turner syndrome. Her gonads were removed after the onset of secondary amenorrhea. Histological examination revealed a degenerative right ovary devoid of germ cells and follicles, and a left streak gonad. There was no trace of testicular development in either side.</description><subject>Adolescent</subject><subject>Female</subject><subject>Gonadal Dysgenesis - pathology</subject><subject>Gonadal Dysgenesis, 46,XY - genetics</subject><subject>Gonadal Dysgenesis, 46,XY - pathology</subject><subject>H-Y Antigen - analysis</subject><subject>HLA Antigens - analysis</subject><subject>Humans</subject><subject>Lymphocytes - analysis</subject><subject>Ovary - pathology</subject><subject>Phenotype</subject><issn>0340-6717</issn><issn>1432-1203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1982</creationdate><recordtype>article</recordtype><recordid>eNpF0D1LA0EUheFBlBijjb2wlYW45t753C01GBUCaRS0Wu7O3MjKfsSdJJB_byRBq9M8nOIV4hLhDgHc-GEKYGzuUB6JIWolU5SgjsUQlIbUOnSn4izGLwA0uTQDMXDgrLQ4FOP5hvqK2iTwhutu2XC7Sqo20fb2_SP57FoKVCdhGz-55VjFc3GyoDryxWFH4m36-Dp5Tmfzp5fJ_Sz1MpOrFEl7ygwEAC11hmQcIGaK2RoZMlwQ5FSid4G0lCUqY0rtHXnrg0Un1Uhc73-Xffe95rgqmip6rmtquVvHwmlQeW7NDt7soe-7GHteFMu-aqjfFgjFb53iv84OXx1e12XD4Y8ecqgfQYZcbg</recordid><startdate>19820101</startdate><enddate>19820101</enddate><creator>Russell, M H</creator><creator>Wachtel, S S</creator><creator>Davis, B W</creator><creator>Cahill, L T</creator><creator>Groos, E</creator><creator>Niblack, G D</creator><creator>Burr, I M</creator><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>19820101</creationdate><title>Ovarian development in 46,XY gonadal dysgenesis</title><author>Russell, M H ; Wachtel, S S ; Davis, B W ; Cahill, L T ; Groos, E ; Niblack, G D ; Burr, I M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c282t-1a4ca850d0042481a5701183ee652d81fa09ab1c7da422b1355b4c7ac6cd61723</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1982</creationdate><topic>Adolescent</topic><topic>Female</topic><topic>Gonadal Dysgenesis - pathology</topic><topic>Gonadal Dysgenesis, 46,XY - genetics</topic><topic>Gonadal Dysgenesis, 46,XY - pathology</topic><topic>H-Y Antigen - analysis</topic><topic>HLA Antigens - analysis</topic><topic>Humans</topic><topic>Lymphocytes - analysis</topic><topic>Ovary - pathology</topic><topic>Phenotype</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Russell, M H</creatorcontrib><creatorcontrib>Wachtel, S S</creatorcontrib><creatorcontrib>Davis, B W</creatorcontrib><creatorcontrib>Cahill, L T</creatorcontrib><creatorcontrib>Groos, E</creatorcontrib><creatorcontrib>Niblack, G D</creatorcontrib><creatorcontrib>Burr, I M</creatorcontrib><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>Human genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Russell, M H</au><au>Wachtel, S S</au><au>Davis, B W</au><au>Cahill, L T</au><au>Groos, E</au><au>Niblack, G D</au><au>Burr, I M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ovarian development in 46,XY gonadal dysgenesis</atitle><jtitle>Human genetics</jtitle><addtitle>Hum Genet</addtitle><date>1982-01-01</date><risdate>1982</risdate><volume>60</volume><issue>2</issue><spage>196</spage><epage>199</epage><pages>196-199</pages><issn>0340-6717</issn><eissn>1432-1203</eissn><abstract>In humans the XY ovary is degenerative, there being scant evidence of persistence of that organ beyond the perinatal period. Here we describe indications of functional ovarian tissue in a 17-year-old female with male karyotype, H-Y+ cellular phenotype, and some signs of the Turner syndrome. Her gonads were removed after the onset of secondary amenorrhea. Histological examination revealed a degenerative right ovary devoid of germ cells and follicles, and a left streak gonad. There was no trace of testicular development in either side.</abstract><cop>Germany</cop><pmid>7076261</pmid><doi>10.1007/BF00569712</doi><tpages>4</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0340-6717
ispartof Human genetics, 1982-01, Vol.60 (2), p.196-199
issn 0340-6717
1432-1203
language eng
recordid cdi_proquest_miscellaneous_74039965
source SpringerLink_过刊(NSTL购买)
subjects Adolescent
Female
Gonadal Dysgenesis - pathology
Gonadal Dysgenesis, 46,XY - genetics
Gonadal Dysgenesis, 46,XY - pathology
H-Y Antigen - analysis
HLA Antigens - analysis
Humans
Lymphocytes - analysis
Ovary - pathology
Phenotype
title Ovarian development in 46,XY gonadal dysgenesis
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T09%3A37%3A11IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Ovarian%20development%20in%2046,XY%20gonadal%20dysgenesis&rft.jtitle=Human%20genetics&rft.au=Russell,%20M%20H&rft.date=1982-01-01&rft.volume=60&rft.issue=2&rft.spage=196&rft.epage=199&rft.pages=196-199&rft.issn=0340-6717&rft.eissn=1432-1203&rft_id=info:doi/10.1007/BF00569712&rft_dat=%3Cproquest_cross%3E74039965%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c282t-1a4ca850d0042481a5701183ee652d81fa09ab1c7da422b1355b4c7ac6cd61723%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=74039965&rft_id=info:pmid/7076261&rfr_iscdi=true