Congenital Cranial Dysinnervation Disorders

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.

Year introduced: 2023

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Do not include MeSH terms found below this term in the MeSH hierarchy.

Tree Number(s): C10.292.562.700.375, C10.500.198, C11.590.436.400, C16.131.666.198

MeSH Unique ID: D000093922

Entry Terms:

• Congenital Fibrosis Syndromes
• Congenital Fibrosis Syndrome
• Congenital Cranial Dysinnervation Syndromes
• Congenital Innervation Dysgenesis Syndrome

Previous Indexing:

• Ocular Motility Disorders (2003-2022)

All MeSH Categories
Diseases Category
Nervous System Diseases
Cranial Nerve Diseases
Ocular Motility Disorders
Oculomotor Nerve Diseases
Congenital Cranial Dysinnervation Disorders
Duane Retraction Syndrome
Mobius Syndrome
Septo-Optic Dysplasia

All MeSH Categories
Diseases Category
Nervous System Diseases
Nervous System Malformations
Congenital Cranial Dysinnervation Disorders

All MeSH Categories
Diseases Category
Eye Diseases
Ocular Motility Disorders
Oculomotor Nerve Diseases
Congenital Cranial Dysinnervation Disorders
Duane Retraction Syndrome
Mobius Syndrome
Septo-Optic Dysplasia

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Nervous System Malformations
Congenital Cranial Dysinnervation Disorders