DAX-1 (NR0B1) and steroidogenic factor-1 (SF-1, NR5A1) in human disease

DAX-1 (NR0B1) and SF-1 (NR5A1) are two nuclear receptor transcription factors that play a key role in human adrenal and reproductive development. Loss of DAX-1 function is classically associated with X-linked adrenal hypoplasia congenita. This condition typically affects boys and presents as primary...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Baillière's best practice & research. Clinical endocrinology & metabolism 2015-08, Vol.29 (4), p.607-619
Hauptverfasser: Suntharalingham, Jenifer P., BSc, Buonocore, Federica, PhD, Duncan, Andrew J., PhD, Achermann, John C., MB, MD, PhD, FRCP, FRCPCH
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 619
container_issue 4
container_start_page 607
container_title Baillière's best practice & research. Clinical endocrinology & metabolism
container_volume 29
creator Suntharalingham, Jenifer P., BSc
Buonocore, Federica, PhD
Duncan, Andrew J., PhD
Achermann, John C., MB, MD, PhD, FRCP, FRCPCH
description DAX-1 (NR0B1) and SF-1 (NR5A1) are two nuclear receptor transcription factors that play a key role in human adrenal and reproductive development. Loss of DAX-1 function is classically associated with X-linked adrenal hypoplasia congenita. This condition typically affects boys and presents as primary adrenal insufficiency in early infancy or childhood, hypogonadotropic hypogonadism at puberty and impaired spermatogenesis. Late onset forms of this condition and variant phenotypes are increasingly recognized. In contrast, disruption of SF-1 only rarely causes adrenal insufficiency, usually in combination with testicular dysgenesis. Variants in SF-1/ NR5A1 more commonly cause a spectrum of reproductive phenotypes ranging from 46,XY DSD (partial testicular dysgenesis or reduced androgen production) and hypospadias to male factor infertility or primary ovarian insufficiency. Making a specific diagnosis of DAX-1 or SF-1 associated conditions is important for long-term monitoring of endocrine and reproductive function, appropriate genetic counselling for family members, and for providing appropriate informed support for young people.
doi_str_mv 10.1016/j.beem.2015.07.004
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5159745</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1521690X15000718</els_id><sourcerecordid>1707554806</sourcerecordid><originalsourceid>FETCH-LOGICAL-c510t-efe73350d897589299c2c22c34c9fee2217a7de8727b4735bfe05e9d6d6461a23</originalsourceid><addsrcrecordid>eNp9ktFr1TAUxos43Jz-Az5IHyfYek7SNC3I4DrdJowJm8LeQm5yuuXaNlvSDvbfm3LnUB98SiDf9-Xw_U6WvUEoEbD-sCnXREPJAEUJsgSonmV72MimQNFWz9NdMCzqFq52s5cxbgAAOeCLbJfVHDg0ci87-by6KjA_OL-AT_gu16PN40TBO-uvaXQm77SZfFgkl8cFvs_PL8QqCd2Y38yDHnPrIulIr7KdTveRXj-e-9mP4y_fj06Ls28nX49WZ4URCFNBHUnOBdimlaJpWdsaZhgzvDJtR8QYSi0tNZLJdSW5WHcEglpb27qqUTO-nx1uc2_n9UDW0DgF3avb4AYdHpTXTv39Mrobde3vlUidyEqkgIPHgODvZoqTGlw01Pd6JD9HhRKkEFUDdZKyrdQEH2Og7ukbBLUQUBu1EFALAQVSJQLJ9PbPAZ8svytPgo9bAaWa7h0FFY2j0ZB1gcykrHf_zz_8x256l0Dp_ic9UNz4OYwJgEIVmQJ1uezAsgIoEn6JDf8FxRmoXA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1707554806</pqid></control><display><type>article</type><title>DAX-1 (NR0B1) and steroidogenic factor-1 (SF-1, NR5A1) in human disease</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><creator>Suntharalingham, Jenifer P., BSc ; Buonocore, Federica, PhD ; Duncan, Andrew J., PhD ; Achermann, John C., MB, MD, PhD, FRCP, FRCPCH</creator><creatorcontrib>Suntharalingham, Jenifer P., BSc ; Buonocore, Federica, PhD ; Duncan, Andrew J., PhD ; Achermann, John C., MB, MD, PhD, FRCP, FRCPCH</creatorcontrib><description>DAX-1 (NR0B1) and SF-1 (NR5A1) are two nuclear receptor transcription factors that play a key role in human adrenal and reproductive development. Loss of DAX-1 function is classically associated with X-linked adrenal hypoplasia congenita. This condition typically affects boys and presents as primary adrenal insufficiency in early infancy or childhood, hypogonadotropic hypogonadism at puberty and impaired spermatogenesis. Late onset forms of this condition and variant phenotypes are increasingly recognized. In contrast, disruption of SF-1 only rarely causes adrenal insufficiency, usually in combination with testicular dysgenesis. Variants in SF-1/ NR5A1 more commonly cause a spectrum of reproductive phenotypes ranging from 46,XY DSD (partial testicular dysgenesis or reduced androgen production) and hypospadias to male factor infertility or primary ovarian insufficiency. Making a specific diagnosis of DAX-1 or SF-1 associated conditions is important for long-term monitoring of endocrine and reproductive function, appropriate genetic counselling for family members, and for providing appropriate informed support for young people.</description><identifier>ISSN: 1521-690X</identifier><identifier>EISSN: 1878-1594</identifier><identifier>DOI: 10.1016/j.beem.2015.07.004</identifier><identifier>PMID: 26303087</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>46,XY disorders of sex development ; Addison disease ; Adrenal Insufficiency - genetics ; Adrenal Insufficiency - metabolism ; Adrenal Insufficiency - pathology ; DAX-1 ; DAX-1 Orphan Nuclear Receptor - genetics ; DAX-1 Orphan Nuclear Receptor - metabolism ; Endocrinology &amp; Metabolism ; Genetic Diseases, X-Linked - genetics ; Genetic Diseases, X-Linked - metabolism ; Genetic Diseases, X-Linked - pathology ; Humans ; Hypoadrenocorticism, Familial ; hypogonadotropic hypogonadism ; hypospadias ; infertility ; Male ; Mutation ; Phenotype ; primary adrenal insufficiency ; primary ovarian insufficiency ; SF-1 ; Steroidogenic Factor 1 - genetics ; Steroidogenic Factor 1 - metabolism ; X-linked adrenal hypoplasia congenita</subject><ispartof>Baillière's best practice &amp; research. Clinical endocrinology &amp; metabolism, 2015-08, Vol.29 (4), p.607-619</ispartof><rights>The Authors</rights><rights>2015 The Authors</rights><rights>Copyright © 2015 The Authors. Published by Elsevier Ltd.. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c510t-efe73350d897589299c2c22c34c9fee2217a7de8727b4735bfe05e9d6d6461a23</citedby><cites>FETCH-LOGICAL-c510t-efe73350d897589299c2c22c34c9fee2217a7de8727b4735bfe05e9d6d6461a23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.beem.2015.07.004$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26303087$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Suntharalingham, Jenifer P., BSc</creatorcontrib><creatorcontrib>Buonocore, Federica, PhD</creatorcontrib><creatorcontrib>Duncan, Andrew J., PhD</creatorcontrib><creatorcontrib>Achermann, John C., MB, MD, PhD, FRCP, FRCPCH</creatorcontrib><title>DAX-1 (NR0B1) and steroidogenic factor-1 (SF-1, NR5A1) in human disease</title><title>Baillière's best practice &amp; research. Clinical endocrinology &amp; metabolism</title><addtitle>Best Pract Res Clin Endocrinol Metab</addtitle><description>DAX-1 (NR0B1) and SF-1 (NR5A1) are two nuclear receptor transcription factors that play a key role in human adrenal and reproductive development. Loss of DAX-1 function is classically associated with X-linked adrenal hypoplasia congenita. This condition typically affects boys and presents as primary adrenal insufficiency in early infancy or childhood, hypogonadotropic hypogonadism at puberty and impaired spermatogenesis. Late onset forms of this condition and variant phenotypes are increasingly recognized. In contrast, disruption of SF-1 only rarely causes adrenal insufficiency, usually in combination with testicular dysgenesis. Variants in SF-1/ NR5A1 more commonly cause a spectrum of reproductive phenotypes ranging from 46,XY DSD (partial testicular dysgenesis or reduced androgen production) and hypospadias to male factor infertility or primary ovarian insufficiency. Making a specific diagnosis of DAX-1 or SF-1 associated conditions is important for long-term monitoring of endocrine and reproductive function, appropriate genetic counselling for family members, and for providing appropriate informed support for young people.</description><subject>46,XY disorders of sex development</subject><subject>Addison disease</subject><subject>Adrenal Insufficiency - genetics</subject><subject>Adrenal Insufficiency - metabolism</subject><subject>Adrenal Insufficiency - pathology</subject><subject>DAX-1</subject><subject>DAX-1 Orphan Nuclear Receptor - genetics</subject><subject>DAX-1 Orphan Nuclear Receptor - metabolism</subject><subject>Endocrinology &amp; Metabolism</subject><subject>Genetic Diseases, X-Linked - genetics</subject><subject>Genetic Diseases, X-Linked - metabolism</subject><subject>Genetic Diseases, X-Linked - pathology</subject><subject>Humans</subject><subject>Hypoadrenocorticism, Familial</subject><subject>hypogonadotropic hypogonadism</subject><subject>hypospadias</subject><subject>infertility</subject><subject>Male</subject><subject>Mutation</subject><subject>Phenotype</subject><subject>primary adrenal insufficiency</subject><subject>primary ovarian insufficiency</subject><subject>SF-1</subject><subject>Steroidogenic Factor 1 - genetics</subject><subject>Steroidogenic Factor 1 - metabolism</subject><subject>X-linked adrenal hypoplasia congenita</subject><issn>1521-690X</issn><issn>1878-1594</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9ktFr1TAUxos43Jz-Az5IHyfYek7SNC3I4DrdJowJm8LeQm5yuuXaNlvSDvbfm3LnUB98SiDf9-Xw_U6WvUEoEbD-sCnXREPJAEUJsgSonmV72MimQNFWz9NdMCzqFq52s5cxbgAAOeCLbJfVHDg0ci87-by6KjA_OL-AT_gu16PN40TBO-uvaXQm77SZfFgkl8cFvs_PL8QqCd2Y38yDHnPrIulIr7KdTveRXj-e-9mP4y_fj06Ls28nX49WZ4URCFNBHUnOBdimlaJpWdsaZhgzvDJtR8QYSi0tNZLJdSW5WHcEglpb27qqUTO-nx1uc2_n9UDW0DgF3avb4AYdHpTXTv39Mrobde3vlUidyEqkgIPHgODvZoqTGlw01Pd6JD9HhRKkEFUDdZKyrdQEH2Og7ukbBLUQUBu1EFALAQVSJQLJ9PbPAZ8svytPgo9bAaWa7h0FFY2j0ZB1gcykrHf_zz_8x256l0Dp_ic9UNz4OYwJgEIVmQJ1uezAsgIoEn6JDf8FxRmoXA</recordid><startdate>20150801</startdate><enddate>20150801</enddate><creator>Suntharalingham, Jenifer P., BSc</creator><creator>Buonocore, Federica, PhD</creator><creator>Duncan, Andrew J., PhD</creator><creator>Achermann, John C., MB, MD, PhD, FRCP, FRCPCH</creator><general>Elsevier Ltd</general><scope>6I.</scope><scope>AAFTH</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><scope>5PM</scope></search><sort><creationdate>20150801</creationdate><title>DAX-1 (NR0B1) and steroidogenic factor-1 (SF-1, NR5A1) in human disease</title><author>Suntharalingham, Jenifer P., BSc ; Buonocore, Federica, PhD ; Duncan, Andrew J., PhD ; Achermann, John C., MB, MD, PhD, FRCP, FRCPCH</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c510t-efe73350d897589299c2c22c34c9fee2217a7de8727b4735bfe05e9d6d6461a23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>46,XY disorders of sex development</topic><topic>Addison disease</topic><topic>Adrenal Insufficiency - genetics</topic><topic>Adrenal Insufficiency - metabolism</topic><topic>Adrenal Insufficiency - pathology</topic><topic>DAX-1</topic><topic>DAX-1 Orphan Nuclear Receptor - genetics</topic><topic>DAX-1 Orphan Nuclear Receptor - metabolism</topic><topic>Endocrinology &amp; Metabolism</topic><topic>Genetic Diseases, X-Linked - genetics</topic><topic>Genetic Diseases, X-Linked - metabolism</topic><topic>Genetic Diseases, X-Linked - pathology</topic><topic>Humans</topic><topic>Hypoadrenocorticism, Familial</topic><topic>hypogonadotropic hypogonadism</topic><topic>hypospadias</topic><topic>infertility</topic><topic>Male</topic><topic>Mutation</topic><topic>Phenotype</topic><topic>primary adrenal insufficiency</topic><topic>primary ovarian insufficiency</topic><topic>SF-1</topic><topic>Steroidogenic Factor 1 - genetics</topic><topic>Steroidogenic Factor 1 - metabolism</topic><topic>X-linked adrenal hypoplasia congenita</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Suntharalingham, Jenifer P., BSc</creatorcontrib><creatorcontrib>Buonocore, Federica, PhD</creatorcontrib><creatorcontrib>Duncan, Andrew J., PhD</creatorcontrib><creatorcontrib>Achermann, John C., MB, MD, PhD, FRCP, FRCPCH</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Baillière's best practice &amp; research. Clinical endocrinology &amp; metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Suntharalingham, Jenifer P., BSc</au><au>Buonocore, Federica, PhD</au><au>Duncan, Andrew J., PhD</au><au>Achermann, John C., MB, MD, PhD, FRCP, FRCPCH</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>DAX-1 (NR0B1) and steroidogenic factor-1 (SF-1, NR5A1) in human disease</atitle><jtitle>Baillière's best practice &amp; research. Clinical endocrinology &amp; metabolism</jtitle><addtitle>Best Pract Res Clin Endocrinol Metab</addtitle><date>2015-08-01</date><risdate>2015</risdate><volume>29</volume><issue>4</issue><spage>607</spage><epage>619</epage><pages>607-619</pages><issn>1521-690X</issn><eissn>1878-1594</eissn><abstract>DAX-1 (NR0B1) and SF-1 (NR5A1) are two nuclear receptor transcription factors that play a key role in human adrenal and reproductive development. Loss of DAX-1 function is classically associated with X-linked adrenal hypoplasia congenita. This condition typically affects boys and presents as primary adrenal insufficiency in early infancy or childhood, hypogonadotropic hypogonadism at puberty and impaired spermatogenesis. Late onset forms of this condition and variant phenotypes are increasingly recognized. In contrast, disruption of SF-1 only rarely causes adrenal insufficiency, usually in combination with testicular dysgenesis. Variants in SF-1/ NR5A1 more commonly cause a spectrum of reproductive phenotypes ranging from 46,XY DSD (partial testicular dysgenesis or reduced androgen production) and hypospadias to male factor infertility or primary ovarian insufficiency. Making a specific diagnosis of DAX-1 or SF-1 associated conditions is important for long-term monitoring of endocrine and reproductive function, appropriate genetic counselling for family members, and for providing appropriate informed support for young people.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>26303087</pmid><doi>10.1016/j.beem.2015.07.004</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1521-690X
ispartof Baillière's best practice & research. Clinical endocrinology & metabolism, 2015-08, Vol.29 (4), p.607-619
issn 1521-690X
1878-1594
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5159745
source MEDLINE; Elsevier ScienceDirect Journals Complete
subjects 46,XY disorders of sex development
Addison disease
Adrenal Insufficiency - genetics
Adrenal Insufficiency - metabolism
Adrenal Insufficiency - pathology
DAX-1
DAX-1 Orphan Nuclear Receptor - genetics
DAX-1 Orphan Nuclear Receptor - metabolism
Endocrinology & Metabolism
Genetic Diseases, X-Linked - genetics
Genetic Diseases, X-Linked - metabolism
Genetic Diseases, X-Linked - pathology
Humans
Hypoadrenocorticism, Familial
hypogonadotropic hypogonadism
hypospadias
infertility
Male
Mutation
Phenotype
primary adrenal insufficiency
primary ovarian insufficiency
SF-1
Steroidogenic Factor 1 - genetics
Steroidogenic Factor 1 - metabolism
X-linked adrenal hypoplasia congenita
title DAX-1 (NR0B1) and steroidogenic factor-1 (SF-1, NR5A1) in human disease
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T11%3A02%3A57IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=DAX-1%20(NR0B1)%20and%20steroidogenic%20factor-1%20(SF-1,%20NR5A1)%20in%20human%20disease&rft.jtitle=Bailli%C3%A8re's%20best%20practice%20&%20research.%20Clinical%20endocrinology%20&%20metabolism&rft.au=Suntharalingham,%20Jenifer%20P.,%20BSc&rft.date=2015-08-01&rft.volume=29&rft.issue=4&rft.spage=607&rft.epage=619&rft.pages=607-619&rft.issn=1521-690X&rft.eissn=1878-1594&rft_id=info:doi/10.1016/j.beem.2015.07.004&rft_dat=%3Cproquest_pubme%3E1707554806%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1707554806&rft_id=info:pmid/26303087&rft_els_id=S1521690X15000718&rfr_iscdi=true