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Hydrocephalus obesity hypogonadism

Introduction

Synonyms and keywords: Sengers-Hamel-Otten syndrome

Overview

Overview

This syndrome is characterized by the association of[1]Congenital hydrocephalus, Centripetal obesity, Hypogonadism, Intellectual deficit and Short stature.

Pathophysiology

Pathophysiology

Genetics

An X-linked recessive mode of inheritance was suggested.

Epidemiology and Demographics

Epidemiology and Demographics

It has been described in two males from one family.

References

References

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Assosciate Editor(s)-In-Chief: Prashanth Saddala M.B.B.S