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Hereditary spastic paraplegia 31
30 years). In some cases, it can present as a complex phenotype with additional associated manifestations including peripheral neuropathy, bulbar palsy (with dysarthria and dysphagia), distal amyotrophy, and impaired distal vibration sense.
Pronunciation
/hɪˈrɛdɪtəri ˈspastɪk ˌparəˈpliːʤə 31/
/həˈrɛdəˌtɛri ˈspæstɪk ˌpɛrəˈpliʤiə 31/
Categories
hereditary spastic paraplegia
rare disease