Medicine:Corneal-cerebellar syndrome
| Corneal-cerebellar syndrome | |
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| Other names | Der Kaloustian-Jarudi-Khoury syndrome, corneal dystrophy with spinocebellar degeneration and spinocerebellar degeneration-corneal dystrophy syndrome |
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| Corneal-cerebellar syndrome is inherited in an autosomal recessive manner | |
Corneal-cerebellar syndrome (also known as Der Kaloustian-Jarudi-Khoury syndrome) is an autosomally recessive disease that was first described in 1985.[1][2] Three cases are known: all are sisters in the same family.[1]
Symptoms and signs
The age of onset is in a child's infancy.[1] Bilateral corneal opacification started in the second year of life and led to severe visual impairment. However, cornea surgery and replacement resulted in better vision.[2]
Symptoms include a combination of spinocerebellar degeneration and corneal dystrophy. Mental retardation and slowly progressive cerebellar abnormalities were also diagnosed in patients. Other symptoms include corneal edema, thickening of Descemet membrane, and degenerative pannus. Abnormalities were found in muscle and sural nerves.[2]
Cause
Diagnosis
Differential diagnosis
It was concluded by Mousa-Al et al. that the disease is different from a disease known as spastic ataxia-corneal dystrophy syndrome that had been found a year later in 1986 in an inbred Bedouin family.[2] Corneal-cerebellar syndrome differs from the spastic ataxia-corneal dystrophy syndrome by causing intellectual disability. Corneal dystrophy is also epithelian instead of being stromal.[1]
Treatment
See also
References
Further reading
- "Familial spinocerebellar degeneration with corneal dystrophy". Am. J. Med. Genet. 20 (2): 325–39. 1985. doi:10.1002/ajmg.1320200216. PMID 3872072.
- "Autosomally inherited recessive spastic ataxia, macular corneal dystrophy, congenital cataracts, myopia and vertically oval temporally tilted discs. Report of a Bedouin family—a new syndrome". J. Neurol. Sci. 76 (1): 105–21. 1986. doi:10.1016/0022-510x(86)90145-0. PMID 3465874.
External links
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