Foveal hypoplasia in parents of patients with albinism-Reference-Cited by-同舟云学术

Foveal hypoplasia in parents of patients with albinism

Published:2022-09-13 Issue:6 Volume:43 Page:817-823
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Lejoyeux R.¹,Alonso A-S²,Lafolie J.²,Michaud V.³^ORCID,Lasseaux E.³^ORCID,Vasseur V.²,Derrien S.¹²,Robert M. P.⁴,Le Mer Y.¹,Tadayoni R.¹,Arveiler B.³^ORCID,Mauget-Faÿsse M.¹²

Affiliation:

1. Departement of Retina, Rothschild Foundation hospital, Paris, France

2. Departement of Retina, Centre d’investigation clinique, Paris, France

3. CHU de Bordeaux, Hôpital Pellegrin, Bordeaux, France

4. Department of ophthalmology, Hôpital Necker, APHP, Paris, France

Funder

funding associated with the work featured in this article

Publisher

Informa UK Limited

Subject

Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/13816810.2022.2121841

Reference24 articles.

1. Increasing the complexity: new genes and new types of albinism

2. A Japanese Family With Autosomal Dominant Oculocutaneous Albinism Type 4

3. Structural Grading of Foveal Hypoplasia Using Spectral-Domain Optical Coherence Tomography

4. The superficial and deep retinal capillary plexus in cases of fovea plana imaged by spectral-domain optical coherence tomography angiography

5. The Phenotypic Spectrum of Albinism

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