Structured Summary
Abstract
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.
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Synonyms
4 entry terms
- Congenital Cranial Dysinnervation Syndromes
- Congenital Fibrosis Syndromes
- Congenital Innervation Dysgenesis Syndrome
- Congenital Fibrosis Syndrome
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Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
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History Note
2023
MeSH Record
Previous Indexing
- Ocular Motility Disorders (2003-2022)
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References
- National Library of Medicine. Congenital Cranial Dysinnervation Disorders. Medical Subject Headings (MeSH). 2026. Unique ID D000093922. http://id.nlm.nih.gov/mesh/2026/D000093922
- Congenital Cranial Dysinnervation Disorders. In: Wikidata. https://www.wikidata.org/wiki/Q116758423