Hallermann's Syndrome

An oculomandibulofacial syndrome principally characterized by dyscephaly (usually brachycephaly), parrot nose, mandibular hypoplasia, proportionate nanism, hypotrichosis, bilateral congenital cataracts, and microphthalmia. (Dorland, 27th ed)

Also Known As:

Hallermann Streiff Syndrome; Syndrome, Hallermann-Streiff; Francois Dyscephalic Syndrome; Hallermann Streiff Francois Syndrome; Dyscephalic Syndrome, Francois; Dyscephalic Syndromes, Francois; Francois Dyscephalic Syndromes; Hallermann Syndrome; Hallermanns Syndrome; Syndrome, Francois Dyscephalic; Syndrome, Hallermann's; Syndromes, Francois Dyscephalic; Hallermann-Streiff Syndrome

Musculoskeletal Diseases: 751
- Bone Diseases: 5970
  - Developmental Bone Diseases: 156
    - Dysostoses: 94
      - Craniofacial Dysostosis: 246
        Hallermann's Syndrome: 21
- Musculoskeletal Abnormalities: 46
  - Craniofacial Abnormalities: 208
    - Craniofacial Dysostosis: 246
      - Hallermann's Syndrome: 21
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 960
- Congenital Abnormalities: 26404
  - Musculoskeletal Abnormalities: 46
    - Craniofacial Abnormalities: 208
      - Craniofacial Dysostosis: 246
        Hallermann's Syndrome: 21

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