"Mobius Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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)
| Descriptor ID |
D020331
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| MeSH Number(s) |
C07.465.299.825 C10.292.319.825 C16.131.077.578 C16.614.595
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| Concept/Terms |
Mobius Syndrome- Mobius Syndrome
- Mobius Syndromes
- Congenital Oculofacial Paralysis, Moebius
- Möbius Sequence
- Congenital Ophthalmoplegia and Facial Paresis
- Moebius Sequence
- Moebius Spectrum
- Moebius Syndrome
- Moebius Syndromes
- Moebius Congenital Oculofacial Paralysis
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Below are MeSH descriptors whose meaning is more general than "Mobius Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Mobius Syndrome".
This graph shows the total number of publications written about "Mobius Syndrome" by people in this website by year, and whether "Mobius Syndrome" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2017 | 1 | 0 | 1 |
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Below are the most recent publications written about "Mobius Syndrome" by people in Profiles.
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An exome sequencing study of Moebius syndrome including atypical cases reveals an individual with CFEOM3A and a TUBB3 mutation. Cold Spring Harb Mol Case Stud. 2017 03; 3(2):a000984.
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M?bius syndrome. AJNR Am J Neuroradiol. 2005 Feb; 26(2):430-2.