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

Simple search

*
(*) mandatory field





Other search option(s)

German syndrome

Orpha number ORPHA2077
Prevalence of rare diseases <1 / 1 000 000
Inheritance
  • Autosomal recessive
Age of onset Neonatal/infancy
ICD 10 code -
MIM number
Synonym(s) -

Summary

German syndrome is a very rare association hypotonia-hypokinesia sequence, involving arthrogryposis and lymphedema. Only five cases have been described so far. Three of the four known families with affected children were Ashkenazi Jews. One boy died at age 2 years of cor pulmonale; a girl was stillborn. An autosomal recessive inheritance is likely. *Author: Orphanet (November 2005)*.

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 :