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