Síndrome del microftalmos posterior-drusas papilares-retinosis pigmentaria asociado a puntos blancos. Caso clínico

Author:

Plaza P.,Iturralde O.,Abascal C.

Publisher

Elsevier BV

Subject

Ophthalmology

Reference5 articles.

1. Retinitis pigmentosa, nanophthalmos, and optic disc drusen: A case report;Buys;Ophthalmology.,1999

2. A new autosomal recessive syndrome consisting of posterior microphthalmos, retinitis pigmentosa, foveoschisis, and optic disc drusen is caused by a MFRP gene mutation;Ayala-Ramirez;Mol Vis.,2006

3. A novel mutation confirms MFRP as the gene causing the syndrome of nanophthalmos-renititispigmentosa-foveoschisis-optic disk drusen;Crespi;Am J Ophthlamol.,2008

4. A novel crumbs homolog 1 mutation in a family with retinitis pigmentosa, nanophthalmos, and optic disc drusen;Paun;Mol Vis.,2012

5. Frequency of optic disc or parapapillary nerve fiber layer drusen in retinitis pigmentosa;Grover;Ophthalmology.,1997

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