[Hereditary degenerative spinocerebellar diseases in Tunisia with manometric studies in bladder disorders (author's transl)].

@article{Hamida1980HereditaryDS,
  title={[Hereditary degenerative spinocerebellar diseases in Tunisia with manometric studies in bladder disorders (author's transl)].},
  author={Mongi Ben Hamida and Shahid Madani and Sonja Zmerli and I Chami and A Annabi and M. Jamoussi and Moncef Marzouki and M A Rachdi and S Samoud and Maryam Talbi},
  journal={Revue neurologique},
  year={1980},
  volume={136 8-9},
  pages={495-508}
}
During a survey conducted in Tunisia in 1978, 204 cases of hereditary degenerative spinocerebellar diseases were discovered among members of 117 families. The cases included 109 patients with Friedreich's ataxia, 28 with Piere Marie's heredo-ataxia, 20 with Strumpell-Lorrain's disease, and 47 with intermediary forms. The latter group included incomplete… CONTINUE READING