Rare Zebra

Rare disease search prototype built on Orphanet data

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ORPHA:2077

German syndrome

Also called Hypotonia-arthrogryposis-facial dysmorphism-lymphedema syndrome

Body system
Skin diseases
Inheritance pattern
Autosomal recessive
Typical age of onset
Neonatal
Estimated prevalence
<1 / 1 000 000 (Worldwide)
Rarity class
<1 / 1 000 000

ORPHA:2077 is classified under "Skin diseases" in the Orphanet nomenclature.

Common signs

  • Open mouth
  • Everted lower lip vermilion
  • Brachycephaly
  • Dolichocephaly
  • Micrognathia
  • High forehead