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... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Musculoskeletal Abnormalities > Craniofacial Abnormalities > Craniofacial Dysostosis > Hallermann's Syndrome
Musculoskeletal Diseases > Musculoskeletal Abnormalities > Craniofacial Abnormalities > Craniofacial Dysostosis > Hallermann's Syndrome
... > Musculoskeletal Diseases > Bone Diseases > Bone Diseases, Developmental > Dysostoses > Craniofacial Dysostosis > Hallermann's Syndrome

Preferred term

Hallermann's Syndrome  

Type

  • Topical Descriptor

Broader concept

Entry terms

  • Dyscephalic Syndrome, Francois
  • Dyscephalic Syndromes, Francois
  • Francois Dyscephalic Syndrome
  • Francois Dyscephalic Syndromes
  • Hallermann Streiff Francois Syndrome
  • Hallermann Streiff Syndrome
  • Hallermann-Streiff Syndrome
  • Syndrome, Francois Dyscephalic
  • Syndrome, Hallermann-Streiff
  • Syndromes, Francois Dyscephalic

Note

  • a form of craniofacial dysostosis with other abnorm; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES

Scope note

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

History note

  • 91(65); was see under CRANIOFACIAL DYSOSTOSIS 1985-90; was see under MANDIBULOFACIAL DYSOSTOSIS 1965-84

In other languages

URI

http://www.yso.fi/onto/mesh/D006210

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