17-beta-hydroxysteroid dehydrogenase deficiency physical examination: Difference between revisions
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{{17-beta-hydroxysteroid dehydrogenase deficiency}} | {{17-beta-hydroxysteroid dehydrogenase deficiency}} | ||
{{CMG}} | {{CMG}}; {{AE}} {{Abdulkerim}} | ||
==Overview== | ==Overview== | ||
Majority of affected babies with 17-beta hydroxysteroid dehydrogenase 3 deficiency are born with [[external genitalia]] that appear female. | |||
==Physical Examination== | |||
*Majority of affected babies with 17-beta hydroxysteroid dehydrogenase 3 deficiency are born with external genitalia that appear female. | |||
*In few cases, the external genitalia are [[ambiguous genitalia]]. Some other affected infants have male predominant [[external genitalia]], with small penis [[micropenis]] or [[hypospadias]]. During puberty, the affected individuals develop some male [[secondary sex characteristics]], such as [[increased muscle mass]], [[deepening of the voice]], and development of [[male pattern]] facial and body hair and [[gynecomastia]].<ref name="url17-beta hydroxysteroid dehydrogenase 3 deficiency: MedlinePlus Genetics">{{cite web |url=https://medlineplus.gov/genetics/condition/17-beta-hydroxysteroid-dehydrogenase-3-deficiency/ |title=17-beta hydroxysteroid dehydrogenase 3 deficiency: MedlinePlus Genetics |format= |work= |accessdate=}}</ref> | |||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} | ||
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{{WS}} | {{WS}} | ||
[[Category:Disease]] | [[Category:Disease]] | ||
[[Category:Endocrinology | [[Category:Endocrinology]] | ||
[[Category:Genetic disorders]] | [[Category:Genetic disorders]] | ||
[[Category:needs english review]] | |||
Latest revision as of 07:48, 20 October 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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Diagnosis |
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Treatment |
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Case Studies |
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17-beta-hydroxysteroid dehydrogenase deficiency physical examination On the Web |
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Directions to Hospitals Treating 17-beta-hydroxysteroid dehydrogenase deficiency |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Abdulkerim Yassin, M.B.B.S[2]
Overview
Majority of affected babies with 17-beta hydroxysteroid dehydrogenase 3 deficiency are born with external genitalia that appear female.
Physical Examination
- Majority of affected babies with 17-beta hydroxysteroid dehydrogenase 3 deficiency are born with external genitalia that appear female.
- In few cases, the external genitalia are ambiguous genitalia. Some other affected infants have male predominant external genitalia, with small penis micropenis or hypospadias. During puberty, the affected individuals develop some male secondary sex characteristics, such as increased muscle mass, deepening of the voice, and development of male pattern facial and body hair and gynecomastia.[1]