Olivopontocerebellar atrophy-deafness syndrome
Olivopontocerebellar atrophy-deafness syndrome is a rare genetic disorder characterized by olivopontocerebellar atrophy which begins in infancy, sensorineural hearing loss, and speech delay. Additional findings include cerebellar ataxia. Inheritance pattern varies among families.[1][2][3][4]
| Olivopontocerebellar atrophy-deafness syndrome | |
|---|---|
| Specialty | Medical genetics |
| Complications | Hearing impairment, cerebellar ataxia |
| Usual onset | Infancy |
| Duration | Lifelong |
| Causes | Genetic mutation |
| Risk factors | Being of Omani ancestry |
| Prevention | none |
| Deaths | - |
It has been described in 11 Omani children. The pedigrees of these children couldn't identify a solid mode of inheritance: 8 of the 11 children were suspected to be sporadic cases, while the pedigrees of 3 of the 11 children pointed to autosomal recessive inheritance.[5]
References
- "Olivopontocerebellar atrophy deafness - About the Disease - Genetic and Rare Diseases Information Center". rarediseases.info.nih.gov. Retrieved 2022-07-16.
- RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Search a disease". www.orpha.net. Retrieved 2022-07-16.
- "Olivopontocerebellar Atrophy: Background, Pathophysiology, Epidemiology". 2022-03-11.
{{cite journal}}: Cite journal requires|journal=(help) - Sensory 5. "Olivopontocerebellar atrophy deafness | Rare Diseases". RareGuru. Retrieved 2022-07-16.
- Pratap-Chand, R.; Gururaj, A. K.; Dilip-Kumar, S. (1995-02-01). "A syndrome of olivopontocerebellar atrophy and deafness with onset in infancy". Acta Neurologica Scandinavica. 91 (2): 133–136. doi:10.1111/j.1600-0404.1995.tb00419.x. ISSN 0001-6314. PMID 7785423.
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