par Ohrn Degueldre, C.;Khoubesserian, P.;Toussaint, Daniel 
Référence Bulletin de la Société belge d'ophtalmologie, VOL. 180, page (45-56)
Publication Publié, 1978
Référence Bulletin de la Société belge d'ophtalmologie, VOL. 180, page (45-56)
Publication Publié, 1978
Article révisé par les pairs
| Résumé : | This is a report of a patient with Charcot-Marie-Tooth disease, which was associated both with red color blindness and with retinal pigment degeneration. Study of the family revealed that the neurological condition and the color blindness were both present in the patient's father, and that the mother had retinal degeneration; color blindness was found in one child. The possibility of a combined neurological and ophthalmological transmissible disease in this case is suggested. |
