Congenital Cranial Dysinnervation Disorders [vrozené kraniální dysinervační poruchy]

topical
Terms

syndrom vrozené inervační dysgeneze
syndromy kongenitální fibrózy
vrozené kraniální dysinervační syndromy

 

Congenital Cranial Dysinnervation Syndromes
Congenital Fibrosis Syndromes
Congenital Innervation Dysgenesis Syndrome

Persistent link   https://www.medvik.cz/link/D000093922
Definition

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

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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

C Diseases
C10 Nervous System Diseases 1 884
C10.292 Cranial Nerve Diseases 60
C10.292.562 Ocular Motility Disorders 101
C10.292.562.700 Oculomotor Nerve Diseases 20
C10.292.562.700.250 Adie Syndrome 5
C10.292.562.700.375 Congenital Cranial Dysinnervation Disorders
C10.292.562.700.375.500 Duane Retraction Syndrome 9
C10.292.562.700.375.750 Mobius Syndrome 10
C10.292.562.700.375.875 Septo-Optic Dysplasia 15
C10.292.562.700.500 Oculomotor Nerve Injuries 1
C10.500 Nervous System Malformations 82
C10.500.034 Agenesis of Corpus Callosum 12
C10.500.142 Central Nervous System Cysts 27
C10.500.190 Central Nervous System Vascular Malformations 20
C10.500.198 Congenital Cranial Dysinnervation Disorders
C10.500.205 Dandy-Walker Syndrome 6
C10.500.250 Hereditary Sensory and Autonomic Neuropathies 26
C10.500.300 Hereditary Sensory and Motor Neuropathy 72
C10.500.450 Hydranencephaly 3
C10.500.507 Malformations of Cortical Development 51
C10.500.680 Neural Tube Defects 78
C10.500.760 Optic Nerve Hypoplasia 1
C11 Eye Diseases 1 495
C11.590 Ocular Motility Disorders 101
C11.590.436 Oculomotor Nerve Diseases 20
C11.590.436.200 Adie Syndrome 5
C11.590.436.400 Congenital Cranial Dysinnervation Disorders
C11.590.436.400.500 Duane Retraction Syndrome 9
C11.590.436.400.750 Mobius Syndrome 10
C11.590.436.400.875 Septo-Optic Dysplasia 15
C11.590.436.600 Oculomotor Nerve Injuries 1
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.131 Congenital Abnormalities 1 753
C16.131.666 Nervous System Malformations 82
C16.131.666.034 Agenesis of Corpus Callosum 12
C16.131.666.142 Central Nervous System Cysts 27
C16.131.666.190 Central Nervous System Vascular Malformations 20
C16.131.666.198 Congenital Cranial Dysinnervation Disorders
C16.131.666.205 Dandy-Walker Syndrome 6
C16.131.666.300 Hereditary Sensory and Motor Neuropathy 72
C16.131.666.310 Hereditary Sensory and Autonomic Neuropathies 26
C16.131.666.450 Hydranencephaly 3
C16.131.666.507 Malformations of Cortical Development 51
C16.131.666.680 Neural Tube Defects 78
C16.131.666.763 Optic Nerve Hypoplasia 1

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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

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gaze palsy, familial horizontal, with progressive scoliosis Disease MeSH Browser

monocular elevation deficiency Disease MeSH Browser

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