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Concept information

Nervous System Diseases > Cranial Nerve Diseases > Facial Nerve Diseases > Mobius Syndrome
Stomatognathic Diseases > Mouth Diseases > Facial Nerve Diseases > Mobius Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Abnormalities, Multiple > Mobius Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Infant, Newborn, Diseases > Mobius Syndrome

Terme préférentiel

Mobius Syndrome  

Type

  • mesh:Descriptor

Définition

  • 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)

Concept générique

Concepts associés

Synonyme(s)

  • Congenital Oculofacial Paralysis, Moebius
  • Congenital Ophthalmoplegia and Facial Paresis
  • Möbius Sequence
  • Moebius Congenital Oculofacial Paralysis
  • Moebius Sequence
  • Moebius Spectrum
  • Moebius Syndrome

Qualificatif(s) autorisé(s)

Traductions

  • Syndrome de Moebius

    français

  • Diplégie faciale congénitale
  • Paralysie oculofaciale congénitale de Moebius
  • Syndrome de Mobius

URI

http://data.loterre.fr/ark:/67375/JVR-BFQK9MH4-J

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RDF/XML TURTLE JSON-LD Date de création 08/11/1999, dernière modification le 23/06/2015