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)

Year introduced: 1991(1965)

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Do not include MeSH terms found below this term in the MeSH hierarchy.

Tree Number(s): C05.116.099.370.231.427, C05.660.207.231.427, C16.131.621.207.231.427

MeSH Unique ID: D006210

Entry Terms:

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

All MeSH Categories
Diseases Category
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dysostoses
Craniofacial Dysostosis
Hallermann's Syndrome

All MeSH Categories
Diseases Category
Musculoskeletal Diseases
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Craniofacial Dysostosis
Hallermann's Syndrome

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Craniofacial Dysostosis
Hallermann's Syndrome