FAMILIAL PROGRESSIVE MYOCLONIC EPILEPSY
\famˈɪlɪəl pɹəɡɹˈɛsɪv mˌa͡ɪəklˈɒnɪk ˈɛpɪlˌɛpsi], \famˈɪlɪəl pɹəɡɹˈɛsɪv mˌaɪəklˈɒnɪk ˈɛpɪlˌɛpsi], \f_a_m_ˈɪ_l_ɪ__ə_l p_ɹ_ə_ɡ_ɹ_ˈɛ_s_ɪ_v m_ˌaɪ_ə_k_l_ˈɒ_n_ɪ_k ˈɛ_p_ɪ_l_ˌɛ_p_s_i]\
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A heterogeneous group of primarily familial disorders characterized by myoclonic seizures, tonic-clonic seizures, ataxia, progressive intellectual deterioration, and neuronal degeneration. These include LAFORA DISEASE; MERRF SYNDROME; NEURONAL CEROID-LIPOFUSCINOSIS; sialidosis (see MUCOLIPIDOSES), and UNVERRICHT-LUNDBORG SYNDROME.
By DataStellar Co., Ltd
Word of the day
tinctura quininae ammoniata
- A preparation made by dissolving quinin sulphate in alcohol [Br. Ph.].
Nearby Words
- familial polyneuropathies
- familial polyneuropathy
- familial polyposis coli
- familial polyposis syndrome
- familial polyposis syndromes
- Familial Progressive Myoclonic Epilepsy
- familial retinoblastoma
- familial retinoblastomas
- familial spinocerebellar degeneration
- familial spinocerebellar degenerations
- familial tonic clonic epilepsies