HYPERTROPHIC MOTOR SENSORY NEUROPATHY SPASTIC PARAPLEGIA
\hˌa͡ɪpətɹˈɒfɪk mˈə͡ʊtə sˈɛnsəɹˌi njuːɹˈɒpəθɪ spˈastɪk pˌaɹəplˈiːd͡ʒə], \hˌaɪpətɹˈɒfɪk mˈəʊtə sˈɛnsəɹˌi njuːɹˈɒpəθɪ spˈastɪk pˌaɹəplˈiːdʒə], \h_ˌaɪ_p_ə_t_ɹ_ˈɒ_f_ɪ_k m_ˈəʊ_t_ə s_ˈɛ_n_s_ə_ɹ_ˌi n_j_uː_ɹ_ˈɒ_p_ə_θ_ɪ s_p_ˈa_s_t_ɪ_k p_ˌa_ɹ_ə_p_l_ˈiː_dʒ_ə]\
Definitions of HYPERTROPHIC MOTOR SENSORY NEUROPATHY SPASTIC PARAPLEGIA
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A group of inherited diseases that share similar phenotypes but are genetically diverse. Different genetic loci for autosomal recessive, autosomal dominant, and x-linked forms of hereditary spastic paraplegia have been identified. Clinically, patients present with slowly progessive distal limb weakness and lower extremity spasticity. Peripheral sensory neurons may be affected in the later stages of the disease. (J Neurol Neurosurg Psychiatry 1998 Jan;64 (1):61-6; Curr Opin Neurol 1997 Aug;10 (4):313-8)
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