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Möbius syndrome
Classification and external resources
A child with oromandibular-limb hypogenesis-Möbius syndrome. Notice the expressionless face (due to bilateral VII nerve palsies) and missing fingers.
ICD-10 Q870
ICD-9 352.6
OMIM 157900
DiseasesDB 31978
eMedicine neuro/612
MeSH D020331

Möbius syndrome (also spelled Moebius) (or Congenital ocularfacial paralysis) is an extremely 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. Limb and chest wall abnormalities sometimes occur with the syndrome. Most people with Möbius syndrome have normal intelligence, although their lack of facial expression is sometimes incorrectly taken to be due to dullness or unfriendliness. It is named for Paul Julius Möbius, a neurologist who first described the syndrome in 1888.[1]

Clinical featuresEdit

Möbius syndrome results from the underdevelopment of the VI and VII cranial nerves.[2] The VI cranial nerve controls lateral eye movement, and the VII cranial nerve controls facial expression. People with Möbius syndrome are born with facial paralysis and the inability to move their eyes laterally. Often, the upper lip is retracted due to muscle shrinkage.[3] Occasionally, the cranial nerves V and VIII are affected.[2] If cranial VIII is affected, the person experiences hearing loss.

It is estimated that there are, on average, 2 to 20 cases of Möbius syndrome per million births.[4][5] Although its rarity often leads to late diagnosis, infants with this disorder can be identified at birth by a "mask-like" lack of expression that is detectable during crying or laughing and by an inability to suck while nursing because of paresis (palsy) of the sixth and seventh cranial nerves. Also, because a person with Möbius syndrome cannot follow objects by moving their eyes from side to side, they turn their head instead.

Other symptoms that sometimes occur with Möbius syndrome are:

  • Limb abnormalities—clubbed feet, missing fingers or toes
  • Chest-wall abnormalities (Poland Syndrome)
  • Crossed eyes (strabismus)
  • Difficulty in breathing and/or in swallowing
  • Corneal erosion resulting from difficulty in blinking

Children with Möbius syndrome may have delayed speech because of paralysis of the lips. However, with speech therapy, most people with Möbius syndrome can develop understandable speech.[6] Möbius syndrome has been associated with increased occurrence of the symptoms of autism.[7] However, some children with Möbius syndrome are mistakenly labeled as mentally retarded or autistic because of their expressionless faces, strabismus, and frequent drooling.


There is no single course of medical treatment or cure for Möbius syndrome. Treatment is supportive and in accordance with symptoms. If they have difficulty nursing, infants may require feeding tubes or special bottles to maintain sufficient nutrition. Physical, occupational, and speech therapy can improve motor skills and coordination and can lead to better control of speaking and eating abilities. Often, frequent lubrication with eye drops is sufficient to combat dry eye that results from impaired blinking. Surgery can correct crossed eyes, protect the cornea via tarsorraphy, and improve limb and jaw deformities. Sometimes called smile surgery by the media, muscle transfers grafted from the thigh to the corners of the mouth can be performed to provide the ability to smile. Although "smile surgery" may provide the ability to smile, the procedure is complex and can take twelve hours for each side of the face. Also, the surgery cannot be considered a "cure" for Möbius syndrome, because it does not improve the ability to form other facial expressions.

Social and lifestyle effectsEdit

Möbius syndrome does not prevent individuals from experiencing personal and professional success.[8] Due to the importance of facial expression and smiling in social interaction, the inability to form either can lead to individuals with Möbius being perceived as unfriendly or uninterested in conversations or other social interactions. Individuals who are familiar with Möbius patients such as family or friends can recognize other signals of emotion such as body language, to the point that they sometimes report forgetting that the person has facial paralysis.[9] People with Möbius syndrome can compensate for a lack of expression by using body language, posture, and vocal tone to convey emotion.[10]

Pathological pictureEdit

The causes of Möbius syndrome are poorly understood. Möbius syndrome is thought to result from a vascular disruption (temporary loss of bloodflow) in the brain during prenatal development.[2] There could be many reasons that a vascular disruption leading to Möbius syndrome might occur. Most cases do not appear to be genetic. However, genetic links have been found in a few families. Some maternal trauma may result in impaired or interrupted blood flow (ischemia) or lack of oxygen (hypoxia) to a developing fetus. Some cases are associated with reciprocal translocation between chromosomes or maternal illness. In the majority of cases of Möbius syndrome in which autosomal dominant inheritance is suspected, sixth and seventh cranial nerve paralysis (palsy) occurs without associated limb abnormalities.

The use of drugs and a traumatic pregnancy may also be linked to the development of Mobius syndrome. The use of the drugs misoprostol or thalidomide by women during pregnancy has been linked to the development of Möbius syndrome in some cases. Misoprostol is used to induce abortions in Brazil and Argentina as well as in the United States. Misoprostol abortions are successful 90% of the time, meaning that 10% of the time the pregnancy continues. Studies show that the use of misoprostal during pregnancy increases the risk of developing Möbius syndrome by a factor of 30. While this is a dramatic increase in risk, the incidence of Möbius syndrome without misoprostal use is estimated at one in 50000 to 100000 births (making the incidence of Möbius syndrome with misoprostal use, less than one in 1000 births).[11][12] The use of cocaine (which also has vascular effects) has been implicated in Möbius syndrome.[13]

Some researchers have suggested that the underlying problem of this disorder could be congenital hypoplasia or agenesis of the cranial nerve nuclei. Certain symptoms associated with Möbius syndrome may be caused by incomplete development of facial nerves, other cranial nerves, and other parts of the central nervous system.

Genetic links to 13q12.2[14] and 1p22[15] have been suggested.

Oral/dental concernsEdit

File:MRI of head of Möbius syndrome patient.jpg

Neonatal Edit

When a child is born with Möbius syndrome, there may be difficulty in closing the mouth or swallowing. The tongue may fasciculate (quiver) or be hypotonic (low muscle tone). The tongue may be larger or smaller than average. There may be low tone of the muscles of the soft palate, pharynges, and the masticatory system. The palate may be arched excessively (a high palate), because the tongue does not form a suction that would normally shape the palate down further. The palate may have a groove (this may be partially due to intubation early on if it is for an extended period of time) or may be cleft (incompletely formed). The opening to the mouth may be small. Feeding problems may become a critical issue early on if adequate nutrition is difficult.

Primary dentitionEdit

The primary (baby) teeth generally start coming in by 6 months of age, and all 20 teeth may be in by two and a half years of age. The eruption timing varies greatly. There may be an incomplete formation of the enamel on the teeth (enamel hypoplasia) that makes the teeth more vulnerable to caries (cavities). There may be missing teeth eruptions. If the infant is not closing down properly, the lower jaws become more noticeably deficient (micrognathia or retrognathia). The front teeth may not touch when the child closes down because the back teeth have overerrupted or because of incomplete formation of the maxilla. This condition is called an anterior open bite and has facial/skeletal implications. The saliva may be thick, or the infant may have a dry mouth.

Transitional dentitionEdit

Between age 5 and 7, most children start losing their primary teeth. Occasionally, some primary teeth are slow to exfoliate (fall out), and the dentist may want to remove a primary tooth early to prevent orthodontic problems. Likewise, premature loss of primary teeth may create orthodontic problems later on. When a tooth is lost prematurely, removable or fixed spacers may be needed to prevent the shifting of teeth. Interceptive orthodontic treatment can be initiated at this stage of development to help with crowding or to help relate the upper and lower jaws. Consistent with a high palate is a narrow arch shape of the upper teeth as they line up in the mouth. This may cause the upper front teeth to flare out and become more prone to fracture if accidentally hit. Interceptive orthodontics has an important role in this situation. Appliances that expand the upper arch tend to bring the front teeth back into a more-normal position. Some appliances can even help allow the front teeth to close to normal in an open-bite situation. The mouth and lips may tend to get dry with the Möbius patient. Lack of a good oral seal (lips together) allows the gingiva (gums) to get dry and may get inflamed and irritated.

Permanent dentitionEdit

After the last primary tooth is lost, usually around the age of twelve, final orthodontic treatment can be initiated. A patient that has not been able to close or swallow well probably will have an open bite, deficient lower-jaw growth, a narrow archform with crowded teeth, and upper anterior flaring of teeth. Orthognathic (jaw) surgery may be indicated. This should be completed in most situations before the smile surgery where the gracilis muscle is grafted to the face.

References Edit

  1. Möbius, P. J. (1888). Ueber angeborene doppelseitige Abducens-Facialis-Lahmung. Münchener medizinische Wochenschrift 35: 91–4.
  2. 2.0 2.1 2.2 Briegel W (August 2006). Neuropsychiatric findings of Möbius sequence — a review. Clin. Genet. 70 (2): 91–7.
  3. Al Kaissi A, Grill F, Safi H, Ben Ghachem M, Ben Chehida F, Klaushofer K (2007). Craniocervical junction malformation in a child with Oromandibular-limb hypogenesis-Möbius syndrome. Orphanet J Rare Dis 2: 2.
  4. Kuklík M (2000). Poland-Möbius syndrome and disruption spectrum affecting the face and extremities: a review paper and presentation of five cases. Acta Chir Plast 42 (3): 95–103.
  5. Verzijl HT, van der Zwaag B, Cruysberg JR, Padberg GW (August 2003). Möbius syndrome redefined: a syndrome of rhombencephalic maldevelopment. Neurology 61 (3): 327–33.
  6. Meyerson MD, Foushee DR (June 1978). Speech, language and hearing in Moebius syndrome: a study of 22 patients. Dev Med Child Neurol 20 (3): 357–65.
  7. Gillberg C, Steffenburg S (March 1989). Autistic behaviour in Moebius syndrome. Acta Paediatr Scand 78 (2): 314–6.
  8. Meyerson MD (May 2001). <0231:RASIAW>2.0.CO;2 Resiliency and success in adults with Moebius syndrome. Cleft Palate Craniofac. J. 38 (3): 231–5.
  9. Goldblatt D, Williams D (January 1986). "I an sniling!": Möbius' syndrome inside and out. J. Child Neurol. 1 (1): 71–8.
  10. Bogart KR, Matsumoto D (March 2010). Living with moebius syndrome: adjustment, social competence, and satisfaction with life. Cleft Palate Craniofac. J. 47 (2): 134–42.
  11. Koren G, Schuler L (May 2001). Taking drugs during pregnancy. How safe are the unsafe?. Can Fam Physician 47: 951–3.
  12. Pastuszak AP (1998). Use of Misoprostol during pregnancy and Möbius' syndrome in infants. N Engl J Med 338 (26): 1881–5.
  13. Puvabanditsin S, Garrow E, Augustin G, Titapiwatanakul R, Kuniyoshi KM (April 2005). Poland-Möbius syndrome and cocaine abuse: a relook at vascular etiology. Pediatr. Neurol. 32 (4): 285–7.
  14. Slee JJ, Smart RD, Viljoen DL (June 1991). Deletion of chromosome 13 in Moebius syndrome. J. Med. Genet. 28 (6): 413–414.
  15. Nishikawa M, Ichiyama T, Hayashi T, Furukawa S (February 1997). Möbius-like syndrome associated with a 1;2 chromosome translocation. Clin. Genet. 51 (2): 122–123.

External links Edit

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