Hydrocephalus obesity hypogonadism: Difference between revisions
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{{SK}} Sengers-Hamel-Otten syndrome | {{SK}} Sengers-Hamel-Otten syndrome | ||
==Overview== | ==Overview<ref>http://www.orpha.net/consor/cgi-bin/Disease_Search.php?lng=EN&data_id=3137&Disease_Disease_Search_diseaseGroup=Sengers-Hamel-Otten&Disease_Disease_Search_diseaseType=Pat&disease%28s%29/group%20of%20diseases=Hydrocephalus---obesity---hypogonadism--Sengers-Hamel-Otten-syndrome-&title=Hydrocephalus---obesity---hypogonadism--Sengers-Hamel-Otten-syndrome-&search=Disease_Search_Simple</ref>== | ||
This syndrome is characterized by the association of | This syndrome is characterized by the association of | ||
*Congenital [[hydrocephalus]] | *Congenital [[hydrocephalus]] | ||
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*Intellectual deficit and | *Intellectual deficit and | ||
*Short stature | *Short stature | ||
==Pathophysiology== | ==Pathophysiology== | ||
===Genetics=== | ===Genetics=== | ||
Revision as of 18:52, 29 July 2012
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Assosciate Editor(s)-In-Chief: Prashanth Saddala M.B.B.S
Synonyms and keywords: Sengers-Hamel-Otten syndrome
Overview[1]
This syndrome is characterized by the association of
- Congenital hydrocephalus
- Centripetal obesity
- Hypogonadism
- Intellectual deficit and
- Short stature
Pathophysiology
Genetics
An X-linked recessive mode of inheritance was suggested.
Epidemiology and Demographics
It has been described in two males from one family.
References
- ↑ http://www.orpha.net/consor/cgi-bin/Disease_Search.php?lng=EN&data_id=3137&Disease_Disease_Search_diseaseGroup=Sengers-Hamel-Otten&Disease_Disease_Search_diseaseType=Pat&disease%28s%29/group%20of%20diseases=Hydrocephalus---obesity---hypogonadism--Sengers-Hamel-Otten-syndrome-&title=Hydrocephalus---obesity---hypogonadism--Sengers-Hamel-Otten-syndrome-&search=Disease_Search_Simple