Congenital Cranial Dysinnervation Disorders [vrozené kraniální dysinervační poruchy]
- Terms
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syndrom vrozené inervační dysgeneze
syndromy kongenitální fibrózy
vrozené kraniální dysinervační syndromy
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Congenital Cranial Dysinnervation Syndromes
Congenital Fibrosis Syndromes
Congenital Innervation Dysgenesis Syndrome
Congenital neurodevelopmental diseases characterized by abnormal eye, eyelid, and facial movements. Congenital cranial dysinnervation disorders (CCDDs) are caused by abnormal innervation of CRANIAL NERVES (e.g., CNs III, IV and VI) resulting in aplasia or hypoplasia of the ocular and facial musculature involved in EYE MOVEMENTS.
- DUI
- D000093922 MeSH Browser
- CUI
- M000755105
- Previous indexing
- Ocular Motility Disorders (2003-2022)
- History note
- 2023
- Public note
- 2023
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification
- CO
- complications
- DI
- diagnosis
- DG
- diagnostic imaging
- DH
- diet therapy
- DT
- drug therapy
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology
- EH
- ethnology
- ET
- etiology
- GE
- genetics
- HI
- history
- IM
- immunology
- ME
- metabolism
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology
- PP
- physiopathology
- PC
- prevention & control
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery
- TH
- therapy
- UR
- urine
- VE
- veterinary
- VI
- virology
Marcus Gunn phenomenon Disease MeSH Browser
congenital fibrosis of the extraocular muscles Disease MeSH Browser
external ophthalmoplegia, synergistic divergence, jaw winking, and oculocutaneous hypopigmentation Disease MeSH Browser
fibrosis of extraocular muscles, congenital, with synergistic divergence Disease MeSH Browser
fourth cranial nerve palsy, familial congenital Disease MeSH Browser
gaze palsy, familial horizontal, with progressive scoliosis Disease MeSH Browser
monocular elevation deficiency Disease MeSH Browser