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Möbius syndrome or Moebius syndrome is a rare congenital neurological disorder which is characterized by facial paralysis and the inability to move the eyes from side to side. Most people with Möbius syndrome are born with complete facial paralysis and cannot close their eyes or form facial expressions.
Moebius Models, a company that makes plastic scale models. Mobius Motors, a Kenyan car manufacturer; Moebius Syndrome Foundation, a charitable foundation committed to raising awareness and support for those who have the rare congenital disorder Moebius syndrome. Moebius, a gang in the Tokyo Revengers manga
Moebius syndrome is a bilateral facial paralysis resulting from the underdevelopment of the VII cranial nerve (facial nerve), which is present at birth. The VI cranial nerve, which controls lateral eye movement, is also affected, so people with Moebius syndrome cannot form facial expression or move their eyes from side to side.
Also, Möbius syndrome bears his name, which he first described in 1888; and he pointed the way to understanding the cause of the endocrinological disorder Graves' disease. Moebius won a still dubious fame by his pamphlet "On the Physiological Idiocy of Women" (Halle: Marhold 1900).
This page was last edited on 26 September 2023, at 22:00 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
758.0 Down syndrome; 758.1 Patau's syndrome; 758.2 Edward's syndrome; 758.3 Autosomal deletion syndromes 758.31 Cri du chat syndrome; 758.32 Velo-cardio-facial syndrome; 758.33 Other microdeletions. Miller–Dieker syndrome; Smith–Magenis syndrome; 758.4 Balanced autosomal translocation in normal individual; 758.5 Other conditions due to ...
20669 Ensembl ENSG00000168875 ENSMUSG00000053747 UniProt O95416 Q04892 RefSeq (mRNA) NM_004189 NM_011440 RefSeq (protein) NP_004180 NP_035570 Location (UCSC) Chr 3: 137.76 – 137.77 Mb Chr 9: 99.76 – 99.76 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Transcription factor SOX-14 is a protein that in humans is encoded by the SOX14 gene. Function This intronless gene encodes a ...
Acrocephalosyndactyly presents in numerous different subtypes, however, considerable overlap in symptoms occurs. Generally, all forms of acrocephalosyndactyly are characterized by atypical craniofacial, hand, and foot characteristics, such as premature closure of the fibrous joints in between certain bones of the skull, [16] [17] fusion of certain fingers or toes, [16] [18] and/or more than ...