Rare Zebra

Rare disease search prototype built on Orphanet data

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ORPHA:2108

Hallermann-Streiff syndrome

Also called François dyscephalic syndrome, Oculomandibulofacial syndrome

Body system
Skin diseases
Inheritance pattern
Not applicable, Unknown
Typical age of onset
Antenatal, Infancy, Neonatal
Estimated prevalence
Unknown (Worldwide)
Rarity class
Unknown

ORPHA:2108 is classified under "Skin diseases" in the Orphanet nomenclature.

Common signs

  • Abnormality of the dentition
  • Brachycephaly
  • Convex nasal ridge
  • Developmental cataract
  • Microphthalmia
  • Short ribs