NLM Logo

Hallermann's Syndrome MeSH Descriptor Data 2023


MeSH Heading
Hallermann's Syndrome
Tree Number(s)
C05.116.099.370.231.427
C05.660.207.231.427
C16.131.621.207.231.427
Unique ID
D006210
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D006210
Annotation
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)
Entry Term(s)
Francois Dyscephalic Syndrome
Hallermann Streiff Francois Syndrome
Hallermann-Streiff Syndrome
Public MeSH Note
91; was see under CRANIOFACIAL DYSOSTOSIS 1985-90; was see under MANDIBULOFACIAL DYSOSTOSIS 1965-84
History Note
91(65); was see under CRANIOFACIAL DYSOSTOSIS 1985-90; was see under MANDIBULOFACIAL DYSOSTOSIS 1965-84
Date Established
1991/01/01
Date of Entry
1999/01/01
Revision Date
2012/07/03
Hallermann's Syndrome Preferred
page delivered in 0.153s