Hallermann's Syndrome [Hallermannův syndrom]
topical
5
- Terms
-
Francois Dyscephalic Syndrome
Hallermann Streiff Francois Syndrome
Hallermann-Streiff Syndrome
Persistent link
https://www.medvik.cz/link/D006210
Definition
An oculomandibulofacial syndrome principally characterized by dyscephaly (usually brachycephaly), parrot nose, mandibular hypoplasia, proportionate nanism, hypotrichosis, bilateral congenital cataracts, and microphthalmia. (Dorland, 27th ed)
- Annotation
- a form of craniofacial dysostosis with other abnorm; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
- DUI
- D006210 MeSH Browser
- CUI
- M0009760
- History note
- 91(65); was see under CRANIOFACIAL DYSOSTOSIS 1985-90; was see under MANDIBULOFACIAL DYSOSTOSIS 1965-84
- Public note
- 91; was see under CRANIOFACIAL DYSOSTOSIS 1985-90; was see under MANDIBULOFACIAL DYSOSTOSIS 1965-84
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification
- CO
- complications
- DI
- diagnosis 3
- DG
- diagnostic imaging
- DH
- diet therapy
- DT
- drug therapy
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology
- EH
- ethnology
- ET
- etiology 2
- GE
- genetics 1
- HI
- history
- IM
- immunology
- ME
- metabolism
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology 2
- PP
- physiopathology
- PC
- prevention & control
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery
- TH
- therapy
- UR
- urine
- VE
- veterinary
- VI
- virology
...
Occurrences in Medvik records
C
Diseases
Dennis Fairhurst Moore syndrome Disease MeSH Browser