Sohval-Soffer syndrome: Difference between revisions
Jump to navigation
Jump to search
(Created page with "{{SI}} __NOTOC__ {{CMG}} {{SK}} Male hypergonadotropic hypogonadism - intellectual deficit - skeletal anomalies ==Overview== This syndrome is characterized by [[hypergonadotr...") |
(No difference)
|
Revision as of 23:14, 29 July 2012
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Synonyms and keywords: Male hypergonadotropic hypogonadism - intellectual deficit - skeletal anomalies
Overview
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus.[1]
Epidemiology and Demographics
It has been described in two brothers.
Diagnosis
=Testicular biopsy
Testicular biopsy revealed germinal aplasia and complete seminiferous tubular fibrosis.