Moebius Syndrome

Original Editor - Wendy Walker

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Definition/Description
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Moebius, or Möbius, syndrome is defined as congenital facial palsy combined with abnormal ocular abduction, caused by abnormal development of the 6th and 7th cranial nerves. It is a rare congenital condition that was first described by German neurologist Paul Julius Möbius in 1888[1].

Moebius syndrome is due to the loss of function of motor cranial nerves. Most cases are diagnosed during infancy. The disease is not progressive.

Clinically Relevant Anatomy
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Please see the Facial Nerve and Facial Palsy pages for information on the anatomy of the seventh cranial nerve, AKA facial nerve.

Cranial nerve six, AKA the abducens nerve, innervates the ipsilateral lateral rectus muscle which abducts the ipsilateral eye. The sixth nerve nucleus is located in the pons, just ventral to the floor of the fourth ventricle. Bilateral palsy of the abducens nerve (as seen in Moebius Syndrome) results in lack of eye movement in the horizontal plane, ie. inability to move the eyes laterally. This can be observed by testing lateral tracking of eye movement (keeping the head still) and also when the individual reads text, it is apparent that they have to move their head laterally.

Mechanism of Injury / Pathological Process
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The etiology of Moebius syndrome is not known, but it appears to be multifactorial. There has been evidence of a genetic component related to various loci on chromosomes 3, 10, and 13[2].

The close relationship embryologically between the motor nuclei of the sixth and seventh cranial nerves explains the pathology of this rare condition[3].


Clinical Presentation[edit | edit source]

Bilateral facial immobility/paralysis is the most noticeable symptom, and is frequently noticed very soon after birth, with the parents reporting incomplete eyelid closure during sleep and difficulty sucking (due to lack of lip seal)[4]. However, ooccasionally the facial paralysis is not noticed for a few weeks or months, until the baby's inability to smile or the lack of facial movement with crying arouses the parents' concern. In extremely rare cases the facial paralysis is unilateral.

As the child grows, speech problems emerge due to inability to seal the lips for thee labial consonants. Speech problems are reported in 76-90% of patients with Möbius syndrome[5].

Diagnostic Procedures[edit | edit source]

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Outcome Measures[edit | edit source]

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Management / Interventions
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Differential Diagnosis
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Key Evidence[edit | edit source]

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Resources
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Case Studies[edit | edit source]

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Recent Related Research (from Pubmed)[edit | edit source]

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References[edit | edit source]

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  1. Mobius PJ. Uber angeboren doppelseitige abducens-facialis-lahmung. Munchen Medizinische Wochenschrift. 1888;35:91-4.
  2. Uzumcu A, Karaman B, Toksoy G, Uyguner ZO, Candan S, Eris H. Molecular genetic screening of MBS1 locus on chromosome 13 for microdeletions and exclusion of FGF9, GSH1 and CDX2 as causative genes in patients with Moebius syndrome. Eur J Med Genet. Sep-Oct 2009;52(5):315-20
  3. May M, Schaitkin BM. Facial Nerve Disorders in Newborns and Children. In: The Facial Nerve. 2nd ed. New York, NY: Thieme New York; 2000:339-65
  4. Kumar D. Moebius syndrome. J Med Genet. Feb 1990;27(2):122-6
  5. Briegel W. Neuropsychiatric findings of Mobius sequence -- a review. Clin Genet. Aug 2006;70(2):91-7