Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Jeannette Traoré"'
Autor:
Sanoussi Bamani, Japhet Pobanou Thera, Yakoura H. Abba Kaka, Fatoumata Sylla, Nouhoum Guirou, Seydou Bakayoko, Jeannette Traoré, Amassagou Dougnon
Publikováno v:
Nigerian Journal of Ophthalmology; Vol 26, No 1 (2018)
X-linked juvenile retinoschisis is a hereditary macular dystrophy that is transmitted in the X-linked recessive mode. Clinical signs include a macular star with or without peripheral retinoschisis responsible for decreased visual acuity. This study d
Autor:
Sylla, Fatoumata, Guirou, Nouhom, Napo, Abdoulaye, Simaga, Assiatou, Bakayoko, Seydou, Guindo, Adama, Konandji, Fatimata, Conaré, Ibrahima, Dembélé, Adama, Lamine, Traoré, Jeannette, Traoré
Publikováno v:
Le Mali medical. 32(4)
Juvenile retinoschisis is an inherited macular dystrophy that is transmitted in the chromosome X-linked recessive mode. Clinical signs include a macular star, with or without peripheral retinoschisis, responsible for decreased visual acuity. We repor
Publikováno v:
The Pan African Medical Journal, Vol 26, Iss 123 (2017)
L'édème papillaire est un gonflement liquidien et /ou axonal de la tête du nerf optique du à un blocage du flux axoplasmique au niveau de la lame criblée. Nous rapportons le cas d'une jeune adolescente âgée de 17 ans, qui présenta un édème
Publikováno v:
The Pan African Medical Journal
L'œdème papillaire est un gonflement liquidien et/ou axonal de la tête du nerf optique du à un blocage du flux axoplasmique au niveau de la lame criblée. Nous rapportons le cas d'une jeune adolescente âgée de 17 ans, qui présenta un œdème p
Publikováno v:
Sante (Montrouge, France). 15(4)
The objective of this study was to determine the different groups of ocular disorders causing low vision or blindness among working-age patients consulting at the African Institute of Tropical Ophthalmology (IOTA) in Bamako, Mali.This prospective stu
Publikováno v:
African Journal of Health Sciences; Vol 11, No 1 (2004); 67-69
Gaucher's disease is a recessive autosomal disorder caused by an inherited deficiency of betaglucocerebrosidase. We report here the case of an 8 month old child, fourth in a family of four children, who presents the neuropathic form of the disease. T
Publikováno v:
Journal Français d'Ophtalmologie. 28:213
Autor:
Fatoumata, Sylla, Nouhom, Guirou, Abdoulaye, Napo, Assiatou, Simaga, Seydou, Bakayoko, Adama, Guindo, Fatimata, Konandji, Ibrahima, Conaré, Adama, Dembélé, Lamine, Traoré, Jeannette, Traoré
Publikováno v:
Mali Médical; 2017, Vol. 32 Issue 4, p30-32, 3p