Ataxia telangiectasia in a Bahraini child treated with intensive physiotherapy: A case report
Ataxia telangiectasia (AT) is a rare neurodegenerative condition with a prevalence of 1 in 40,000 to 1 in 300,000 worldwide. It involves a genetic mutation of chromosome 11q.26. The condition is inherited in an autosomal recessive manner causing atrophy of the cerebellum due to loss of Purkinje fibr...
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| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
World Scientific Publishing
2025-06-01
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| Series: | Hong Kong Physiotherapy Journal |
| Subjects: | |
| Online Access: | https://www.worldscientific.com/doi/10.1142/S1013702525710015 |
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