17-beta-hydroxysteroid dehydrogenase deficiency historical perspective: Difference between revisions
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{{17-beta-hydroxysteroid dehydrogenase deficiency}} | {{17-beta-hydroxysteroid dehydrogenase deficiency}} | ||
{{CMG}}; {{AE}} | |||
==Overview== | |||
==Historical Perspective== | |||
17 beta hydroxysteroid dehydrogenase III defiency is initially described in 1971 by [[Saez]] and his colleagues. Patients with [[XY]] [[chromosomes]] usually present at birth with female or [[ambiguous]] [[external genitalia]]. Two important features of this disease are the presence of [[epididymus]], [[vas deferens]], and [[seminal vesicles]] and the progressive [[virilization]] at the time of puberty. To date, At least 20 [[mutations]] have been reported in the 17-beta-HSD type 3 isozyme gene (HSD17B3), localized to [[9q22]]. These are mainly [[missense]]/[[nonsense]] mutations. Genetically, patients can be [[homozygous]] or [[compound heterozygous]].<ref name="pmid17509588">{{cite journal| author=Mains LM, Vakili B, Lacassie Y, Andersson S, Lindqvist A, Rock JA| title=17beta-hydroxysteroid dehydrogenase 3 deficiency in a male pseudohermaphrodite. | journal=Fertil Steril | year= 2008 | volume= 89 | issue= 1 | pages= 228.e13-7 | pmid=17509588 | doi=10.1016/j.fertnstert.2007.02.048 | pmc=2259022 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17509588 }} </ref> | 17 beta hydroxysteroid dehydrogenase III defiency is initially described in 1971 by [[Saez]] and his colleagues. Patients with [[XY]] [[chromosomes]] usually present at birth with female or [[ambiguous]] [[external genitalia]]. Two important features of this disease are the presence of [[epididymus]], [[vas deferens]], and [[seminal vesicles]] and the progressive [[virilization]] at the time of puberty. To date, At least 20 [[mutations]] have been reported in the 17-beta-HSD type 3 isozyme gene (HSD17B3), localized to [[9q22]]. These are mainly [[missense]]/[[nonsense]] mutations. Genetically, patients can be [[homozygous]] or [[compound heterozygous]].<ref name="pmid17509588">{{cite journal| author=Mains LM, Vakili B, Lacassie Y, Andersson S, Lindqvist A, Rock JA| title=17beta-hydroxysteroid dehydrogenase 3 deficiency in a male pseudohermaphrodite. | journal=Fertil Steril | year= 2008 | volume= 89 | issue= 1 | pages= 228.e13-7 | pmid=17509588 | doi=10.1016/j.fertnstert.2007.02.048 | pmc=2259022 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17509588 }} </ref> | ||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} | ||
Revision as of 18:15, 9 May 2022
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17-beta-hydroxysteroid dehydrogenase deficiency Microchapters |
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Differentiating 17-beta-hydroxysteroid dehydrogenase deficiency from other Diseases |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Overview
Historical Perspective
17 beta hydroxysteroid dehydrogenase III defiency is initially described in 1971 by Saez and his colleagues. Patients with XY chromosomes usually present at birth with female or ambiguous external genitalia. Two important features of this disease are the presence of epididymus, vas deferens, and seminal vesicles and the progressive virilization at the time of puberty. To date, At least 20 mutations have been reported in the 17-beta-HSD type 3 isozyme gene (HSD17B3), localized to 9q22. These are mainly missense/nonsense mutations. Genetically, patients can be homozygous or compound heterozygous.[1]
References
- ↑ Mains LM, Vakili B, Lacassie Y, Andersson S, Lindqvist A, Rock JA (2008). "17beta-hydroxysteroid dehydrogenase 3 deficiency in a male pseudohermaphrodite". Fertil Steril. 89 (1): 228.e13–7. doi:10.1016/j.fertnstert.2007.02.048. PMC 2259022. PMID 17509588.