Mobius syndrome
Sign in to saveAlso known as Moebius congenital oculofacial paralysis, Oromandibular-limb hypogenesis spectrum (disorder), Oromandibular-limb hypogenesis spectrum, Möbius Syndrome, MOEBIUS SYNDROME, Moebius Sequence, MBS, Congenital facial diplegia
rare disease
In the Vinony graph
Within Vinony's link graph, Mobius syndrome is referenced by 110 other articles, and connects out to facial paralysis, human pregnancy and medication.
It is catalogued under topics including Genetic disorders with OMIM but no gene, Neurological disorders and Rare syndromes.
Its subject is documented across 25 Wikipedia language editions.
Research
614 papers- Möbius syndrome.Journal of neurosciences in rural practice · 2016
- Möbius syndrome.Seminars in plastic surgery · 2004
- Poland-Möbius syndrome.Journal of medical genetics · 1981
- Poland-Möbius syndrome: a case report implicating a novel mutation of the PLXND1 gene and literature review.BMC pediatrics · 2022
- Möbius syndrome: clinico-radiologic correlation.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2018
via PubMed
Wikidata facts
- Subclass of
- disease
- Named after
- Paul Julius Möbius
- Image
- Infant with Möbius syndrome.jpg
Show 9 more facts
- on focus list of Wikimedia project
- WikiProject Medicine
- discoverer or inventor
- Paul Julius Möbius
- health specialty
- medical genetics
- NCI Thesaurus ID
- C84893
- Commons category
- Möbius syndrome
- exact match
- www.orpha.net/ORDO/Orphanet_570
- symptoms and signs
- facial paralysis
- ICD-9-CM
- 759.89
- external data available at URL
- www.nanbyou.or.jp/entry/5326
via Wikidata · CC0