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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.
numb chin syndrome; numb cheek syndrome; herpes simplex virus infection; facial nerve bell's palsy; bilateral facial palsy; congenital (trauma, Mobius syndrome, cardiofacial syndrome) glossopharyngeal nerve glossopharyngeal neuralgia; glomus jugulare tumor; vagus nerve injury; spinal accessory nerve palsy; hypoglossal nerve injury
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.
Mobius syndrome - a rare congenital disorder in which both VIth and VIIth nerves are bilaterally affected giving rise to a typically 'expressionless' face. 2. Duane syndrome - A condition in which both abduction and adduction are affected arising as a result of partial innervation of the lateral rectus by branches from the IIIrd oculomotor ...
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 is a list of major and frequently observed neurological disorders (e.g., Alzheimer's disease), symptoms (e.g., back pain), signs (e.g., aphasia) and syndromes (e.g., Aicardi syndrome). There is disagreement over the definitions and criteria used to delineate various disorders and whether some of these conditions should be classified as ...
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 ...