Structured Summary
Abstract
A syndrome of congenital facial paralysis, frequently associated with abducens palsy and other congenital abnormalities including lingual palsy, clubfeet, brachial disorders, cognitive deficits, and pectoral muscle defects. Pathologic findings are variable and include brain stem nuclear aplasia, facial nerve aplasia, and facial muscle aplasia, consistent with a multifactorial etiology. (Adams et al., Principles of Neurology, 6th ed, p1020)
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Synonyms
9 entry terms
- Congenital Oculofacial Paralysis, Moebius
- Congenital Ophthalmoplegia and Facial Paresis
- Moebius Congenital Oculofacial Paralysis
- Moebius Sequence
- Moebius Spectrum
- Moebius Syndrome
- Möbius Sequence
- Mobius Syndromes
- Moebius Syndromes
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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.
MeSH Record
History Note
2000; use FACIAL PARALYSIS 1997-1999
MeSH Record
Previous Indexing
- Facial Paralysis (1966-1999)
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References
- National Library of Medicine. Mobius Syndrome. Medical Subject Headings (MeSH). 2026. Unique ID D020331. http://id.nlm.nih.gov/mesh/2026/D020331
- Mobius Syndrome. In: Wikipedia. https://en.wikipedia.org/wiki/Moebius_syndrome
- Mobius Syndrome. In: Wikidata. https://www.wikidata.org/wiki/Q1418152