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Stomatognathic Diseases > Mouth Diseases > Facial Nerve Diseases > Mobius Syndrome
Nervous System Diseases > Cranial Nerve 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
... > Nervous System Diseases > Central Nervous System Diseases > Ocular Motility Disorders > Oculomotor Nerve Diseases > Congenital Cranial Dysinnervation Disorders > Mobius Syndrome
Eye Diseases > Ocular Motility Disorders > Oculomotor Nerve Diseases > Congenital Cranial Dysinnervation Disorders > Mobius Syndrome
... > Nervous System Diseases > Cranial Nerve Diseases > Ocular Motility Disorders > Oculomotor Nerve Diseases > Congenital Cranial Dysinnervation Disorders > Mobius Syndrome
Nervous System Diseases > Nervous System Malformations > Congenital Cranial Dysinnervation Disorders > Mobius Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Nervous System Malformations > Congenital Cranial Dysinnervation Disorders > Mobius Syndrome

Preferred term

Mobius Syndrome  

Type

  • Topical Descriptor

Broader concept

Related concepts

Entry terms

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

Scope note

  • 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)

History note

  • 2000; use FACIAL PARALYSIS 1997-1999

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URI

http://www.yso.fi/onto/mesh/D020331

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