-transparent.png){kind=logo}
Hereditary retinal dystrophies can be subdivised into central (macular) and peripheral degenerations. Stargardt disease, Best disease, cone dystrophy and retinoschisis, affecting children or young adults, are the 4 commonest macular dystrophies. Retinitis pigmentosa, with primary affects photoreceptors, presents a wide clinical, genetic and molecular heterogeneity. It is certainly the most representative cause of peripheral degeneration. Recent advances in molecular biology allow a more complete clinical definition of these inheritable retinal diseases.
Related Publications
E Souied, and
G Soubrane, and
G Coscas
December 1969,
Nederlands tijdschrift voor geneeskunde,
E Souied, and
G Soubrane, and
G Coscas
July 2005,
Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft,
E Souied, and
G Soubrane, and
G Coscas
January 2013,
Journal of ophthalmology,
E Souied, and
G Soubrane, and
G Coscas
August 2005,
Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft,
E Souied, and
G Soubrane, and
G Coscas
September 1973,
The Veterinary clinics of North America,
E Souied, and
G Soubrane, and
G Coscas
January 1996,
Therapeutische Umschau. Revue therapeutique,
E Souied, and
G Soubrane, and
G Coscas
August 2018,
Acta ophthalmologica,
E Souied, and
G Soubrane, and
G Coscas
January 1977,
Bericht uber die Zusammenkunft. Deutsche Ophthalmologische Gesellschaft,
E Souied, and
G Soubrane, and
G Coscas
February 2010,
[Zhonghua yan ke za zhi] Chinese journal of ophthalmology,
E Souied, and
G Soubrane, and
G Coscas
March 2013,
Klinische Monatsblatter fur Augenheilkunde,
