Details

Autor(en) / Beteiligte

• Amaral, Rebeca A S
• Zin, Olivia A
• Moraes, Remo T
• Porto, Fernanda B O
• Carricondo, Pedro C
• Pimentel, Sergio L G
• Kestelman, Bernardo P
• Watanabe, Sung E S
• Sallum, Juliana M F

Titel

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

Ist Teil von

• Ophthalmic genetics, 2024-08, Vol.45 (4), p.1-420

Ort / Verlag

England

Erscheinungsjahr

2024

Beschreibungen/Notizen

• To describe the phenotype and genotype of 10 Brazilian patients with variants in , posterior microphthalmos and retinal findings. Complete ophthalmological evaluation was done at 4 different Brazilian centers. Genetic analysis was performed using commercial next generation sequencing panels for inherited retinal disorders. Ages of the patients ranged from 10 to 65 years and visual acuities from 0,05 to no perception of light. All were hyperopes (+4,25 to + 17,50) with a short axial length (14,4 mm to 18 mm). Common posterior segment features, though not present in all, were optic disc drusen (5/10), foveoschisis (5/10) and retinal pigmentary changes (8/10). Isolated patients presented with macular atrophy, serous retinal detachment, and chorioretinal folds. The most common variant in found in our patients was a deletion in exon 5 (c.498delC; p.Asn267Thrfs *25), present in all except 2 patients. Other variants found were c.523C>T (p.Gln175*), c.298delG (p.Ala100Argfs *37), c.666del (p.Thr223Argfs *83) and the novel variant c.257C>A (p.Ala86Asp). This is the first report of Brazilian patients with posterior microphthalmos and pathogenic variants in and the first describe of the variant p.Ala86Asp in literature. Our cases confirm the previously reported phenotype of high hyperopia, optic disc drusen, alterations in foveal architecture, retinal pigmentary changes with loss of photoreceptor function and visual field constriction. Report of such a rare condition is important to increase awareness to the phenotype of posterior microphthalmia with associated retinal conditions.