Skip to
  1. Homepage
  2. Rare diseases
  3. Search
PrintPrint
Simple search

Simple search

*
(*) mandatory field





Other search option(s)

Cerebral gigantism - jaw cysts

Orpha number ORPHA2081
Prevalence of rare diseases <1 / 1 000 000
Inheritance
  • Unknown
Age of onset -
ICD 10 code -
MIM number -
Synonym(s) Cramer-Niederdellmann syndrome

Summary

This syndrome is characterised by cerebral gigantism associated with a jaw cyst basal cell naevoid syndrome. It has been reported in less than ten patients from two families. Neurological manifestations include hydrocephalus, ventricular malformation, a cerebellar syndrome, intracranial calcification, oculomotor disturbances and, in some cases, mild peripheral nervous disorders. *Author: Orphanet (February 2007)*.

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.
Languages :