Posterior microphthalmos with retinal involvement related to <i>MFRP</i> gene: a report of 10 Brazilian patients-Reference-Cited by-同舟云学术

Posterior microphthalmos with retinal involvement related to MFRP gene: a report of 10 Brazilian patients

Published:2024-04 Issue:4 Volume:45 Page:413-420
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Amaral Rebeca A. S.¹²^ORCID,Zin Olivia A.¹³,Moraes Remo T.³,Porto Fernanda B. O.⁴⁵⁶,Carricondo Pedro C.⁷,Pimentel Sergio L. G.⁷,Kestelman Bernardo P.⁷,Watanabe Sung E. S.¹,Sallum Juliana M. F.¹²^ORCID

Affiliation:

1. Department of Ophthalmology, Federal University of São Paulo, São Paulo, Brazil

2. Instituto de Genética Ocular (IGO), São Paulo, Brazil

3. Brazilian Institute of Ophthalmology (IBOL), Rio de Janeiro, Brazil

4. INRET Clínica e Centro de Pesquisa, Brazil

5. Centro Oftalmológico de Minas Gerais, Brazil

6. Clínica de Olhos da Santa Casa de Belo Horizonte, Brazil

7. Department of Ophthalmology, University of São Paulo, São Paulo, Brazil

Funder

Coordenação de Aperfeiçamento de Nível Superior

Publisher

Informa UK Limited

Link

https://www.tandfonline.com/doi/pdf/10.1080/13816810.2024.2322650

Reference19 articles.

1. Posterior segment changes associated with posterior microphthalmos

2. Developmental Basis of Nanophthalmos:MFRPIs Required for both Prenatal Ocular Growth and Postnatal Emmetropization

3. 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 R;Mol Vis,2006

4. A Novel Mutation Confirms MFRP as the Gene Causing the Syndrome of Nanophthalmos–Renititis Pigmentosa–Foveoschisis–Optic Disk Drusen

5. Retinitis pigmentosa, nanophthalmos, and optic disc drusen