"Hallermann's Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An oculomandibulofacial syndrome principally characterized by dyscephaly (usually brachycephaly), parrot nose, mandibular hypoplasia, proportionate nanism, hypotrichosis, bilateral congenital cataracts, and microphthalmia. (Dorland, 27th ed)
| Descriptor ID |
D006210
|
| MeSH Number(s) |
C05.116.099.370.231.427 C05.660.207.231.427 C16.131.621.207.231.427
|
| Concept/Terms |
Hallermann's Syndrome- Hallermann's Syndrome
- Hallermann Syndrome
- Hallermanns Syndrome
- Syndrome, Hallermann's
- Hallermann Streiff Francois Syndrome
- 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
|
Below are MeSH descriptors whose meaning is more general than "Hallermann's Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Hallermann's Syndrome".
This graph shows the total number of publications written about "Hallermann's Syndrome" by people in this website by year, and whether "Hallermann's Syndrome" was a major or minor topic of these publications.
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Below are the most recent publications written about "Hallermann's Syndrome" by people in Profiles.
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Overarching control of autophagy and DNA damage response by CHD6 revealed by modeling a rare human pathology. Nat Commun. 2021 05 21; 12(1):3014.
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Extensive wormian bones in a patient with the Hallermann-Streiff syndrome. J Child Neurol. 1990 Jan; 5(1):50-1.
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[Hallermann-Streiff syndrome. A case report]. Ann Dermatol Venereol. 1990; 117(3):203-6.