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Factsheet about Cranial Nerve Abnormalities

For a printable version please see: Factsheet about Cranial Nerve Abnormalities


Bruce R. Korf, M.D., Ph.D.
Medical Director, Harvard-Partners Center for Genetics and Genomics 77 Ave Louis Pasteur, Suite 642, Boston, MA 02115
bkorf@partners.org (617) 525-5750

Brain anomalies seen in CHARGE
Cranial nerve anomalies (70-90%)
I – olfactory – (arhinencephaly in 42%) II – optic (colobomas in 80%)
III, IV, V, VI rarely affected
VII – facial palsy, UL or BL (43%) VIII – acoustic (60 – 80%+)
IX, X glossopharyngeal/vagus (50%+) XI accessory – rarely affected
XII hypoglossal – rarely affected

Structural anomalies (less common) agenesis of the corpus callosum arhinencephaly holoprosencephaly hydrocephalus
cerebral dysgenesis Mondini defect hindbrain defects
cerebellar hypoplasia Dandy-Walker malformation


behavior abnormalities learning disabilities

Development: although it has been reported in the past that a majority of children with CHARGE are mentally retarded, this is not necessarily the case. It is extremely important for parents to realize that their child may have significant (even near-normal) potential, given accurate diagnosis and appropriate management of sensory deficits and other complications of CHARGE.

Diagnostic tests/referrals
MRI of brain CT
EEG (if suspect seizures) Evoked potentials (vision/hearing)
Other hearing tests (otolaryngology) Dilated eye exam (ophthalmology)
Developmental testing (developmental pediatrics/deafblind specialist)

Medical treatment caveats
Possible unexpected reaction to anesthesia: Some children with CHARGE are resistant to sedation, while others are slow to recover from anesthesia. Because of risks of anesthesia, it may be appropriate to combine surgical procedures in these children.

Laryngomalacia or tracheomalacia is common in CHARGE and can result in surgical or anesthetic complications. The mortality rate in children with this combination of features is high.

Reflux, facial palsy and other cranial nerve anomalies may additionally compromise feeding in these children. There is a very high risk for repeated aspiration pneumonia.

If MRI is being considered, also consider a few more cuts to view the inner and middle ear, as there is a very high frequency of ossicular malformations and/or Mondini defect.

Non-medical management
Cranial nerve IX, X, and VII anomalies can have an enormous impact on feeding. Feeding issues and common aspiration pneumonia are among the most important day-to-day issues for families. Often a feeding specialist can help the family cope with these issues.


Blake KD, Davenport SLH, Hall BD, Hefner MA, Pagon RA, Williams MS, Lin AE, Graham JM: CHARGE association: an update and review for the primary pediatrician. Clinical Pediatrics 1998;37:159-174.

Byerly K, Pauli RM: Cranial Nerve Abnormalities in CHARGE Association. Am J Med Gen. 1993; 45:751-757

Harvey AS, Leaper PM, Bankier A. CHARGE association: Clinical manifestations and developmental outcome. Am, J Med Genet. 1991; 39:48-55

Lin AE, Siebert JR, Graham JM: Central Nervous System Malformations in the CHARGE Association. Am J Med Genet. 1990; 37: 304-310.


Bruce R. Korf, M.D. Ph.D.
Medical Director, Harvard-Partners Center for Genetics and Genomics 77 Ave Louis Pasteur, Suite 642, Boston, MA 02115
bkorf@partners.org (617) 525-5750 and
Meg Hefner, M.S.
Assistant Professor of Pediatrics, Division of Medical Genetics, St. Louis University School of Medicine, 1465 S. Grand Blvd. St. Louis, MO 63104
Hefnerma@slu.edu or Meg@chargesyndrome.org (314)768-8730

Brain structure:              (top)


Cranial nerves: there are 12 cranial nerves, which begin in the brain and extend to structures in the head and neck. These nerves provide both motor control and sensation and include nerves involved in the senses of smell, taste, hearing, and vision, as well as movements of the eyes, face, tongue, palate, and swallowing. Some cranial nerves are also involved in the control of heart rate and movements of the gastrointestinal tract. Cranial nerve anomalies are very frequent in CHARGE.


AnomalyFrequencyTests UsesSpecialist
I - olfactory (smell)? 40%Clinical assessmentneurologist/otolaryngologist
II - optic nerve Coloboma80-90%Dilated exam Visual evoked responsesOphthalmologist
VII - facial palsy42%, usually one sidedClinical assessmentneurologist
VIII - sensorineural hearing loss60-80%ABR
Other hearing tests
pediatric audiologist otolaryngologist
IX, X swallowing and oromotor problems50%+Barium swallow Laryngoscopyotolaryngologist
OT, PT, speech pathology
XII - tonguerareClinical assessmentneurologist

Structural brain anomalies:

A variety of structural malformations of the brain have been reported in children with CHARGE. Pretty much any brain anomaly is consistent with CHARGE; none are extremely common. A neurologist may order brain imaging such as MRI or CT scan to look for possible structural brain anomalies. Because not all children have had imaging performed, it is not possible to list the frequency of each anomaly.

1. Arhinencephaly: absence of the olfactory lobes
2. Holoprosencephaly: abnormal formation of the cerebral hemispheres.
3. Agenesis of the corpus callosum: lack of fiber tract connecting the two hemispheres.
4. Cerebral dysgenesis: abnormal formation of the cerebral cortex.
5. Hydrocephalus: increased fluid in the ventricles of the brain Other brain abnormalities described in CHARGE
1. Seizures: diagnosed by EEG
2. Behavior abnormalities: See DEVELOPMENT sections
3. Learning disabilities: SEE Development section


Cranial nerve abnormalities: cannot be surgically corrected. Only a few (hearing loss, swallowing problems) are amenable to management.

Olfactory nerve (I):
This nerve controls the sense of smell. If it is abnormal, the child’s sense of smell (and therefore taste) will be absent or abnormal. This can complicate feeding problems.

Optic nerve (II):
A majority of children with CHARGE have colobomas. Optic nerve colobomas can severely affect vision. See EYE section.

Facial palsy (VII):
Droopiness or weakness of one (unilateral, UL) or both sides (bilateral, BL) of the face. This may affect feeding, with drooling on the affected side. If bilateral, there may be problems keeping food in the mouth. Facial palsy can have an effect on facial expression. In some cases, the eye on the affected side may not close completely and need to be kept moist with artificial tears. In some cases, facial nerve palsies get better over time. See FEEDING section.

Acoustic nerve (VIII):
Abnormalities of cranial nerve VIII will result in sensorineural hearing loss (see EARS AND HEARING).

Glossopharyngeal and vagus nerves (IX and X):
These nerves are involved in coordination of suck and swallow and with some of the mouth movements involved in speech. Feeding and swallowing problems are very common in children with CHARGE (see FEEDING). Many of these problems get better over time (often years), due to a combination of maturation of the nerve and use of appropriate therapies.

Structural brain abnormalities: most are not treatable
1. Arhinencephaly will cause lack of smell. This can be difficult to diagnose, but has been described very often at autopsy in CHARGE.

2. Holoprosencephaly is a serious brain abnormality, which is likely to result in significant mental retardation.

3. Agenesis of the corpus callosum is often (but not always) associated with learning disabilities and/or mental retardation.

4. Hydrocephalus can be associated with learning disabilities or mental retardation. Hydrocephalus is treated by placing a shunt.

5. Cerebral dysgenesis: many children with CHARGE have structural brain abnormalities noted on MRI or CT scan. The significance in terms of functioning is not always clear.

Other brain abnormalities described in CHARGE
1. Seizures: diagnosed by EEG, often effectively treated with medication
2. Behavior abnormalities: See DEVELOPMENT sections

Facial Palsy (One Side or Both)
Facial Palsy (One Side or Both)
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