[HTML][HTML] CRB1-associated retinal dystrophies: genetics, clinical characteristics, and natural history
MD Varela, M Georgiou, Y Alswaiti, J Kabbani… - American Journal of …, 2023 - Elsevier
PURPOSE To analyze the clinical characteristics, natural history, and genetics of CRB1-
associated retinal dystrophies. DESIGN Multicenter international retrospective cohort study …
associated retinal dystrophies. DESIGN Multicenter international retrospective cohort study …
Association of Circulating Antiretinal Antibodies With Clinical Outcomes in Retinitis Pigmentosa
L Bianco, A Arrigo, A Antropoli… - … & Visual Science, 2023 - iovs.arvojournals.org
Purpose: To determine if circulating antiretinal antibodies (ARAs) differ between patients
affected by retinitis pigmentosa (RP) and control participants and to assess whether ARAs …
affected by retinitis pigmentosa (RP) and control participants and to assess whether ARAs …
[HTML][HTML] New OCT and OCTA insights in inherited retinal dystrophies
A Arrigo, L Bianco, A Antropoli, A Saladino… - … and Innovations in …, 2023 - intechopen.com
Optical coherence tomography (OCT) and OCT angiography (OCTA) radically changed the
diagnostics of inherited retinal dystrophies (IRD), providing new information regarding the …
diagnostics of inherited retinal dystrophies (IRD), providing new information regarding the …
Unilateral pigmented paravenous retinochoroidal atrophy with acute angle-closure glaucoma: a case report
K Lv, Z Liang, K Yang, X Chen, Y Ma, H Wu - BMC ophthalmology, 2023 - Springer
Background Pigmented paravenous retinochoroidal atrophy (PPRCA) is an uncommon
fundus disease characterized by perivenous aggregations of pigment clumps and …
fundus disease characterized by perivenous aggregations of pigment clumps and …
RPGRIP1 variant associated with pigmented paravenous chorioretinal atrophy
L Bianco, A Antropoli, A Arrigo… - European Journal …, 2023 - journals.sagepub.com
Purpose To report a case of Pigmented Paravenous Chorioretinal Atrophy (PPCRA)
associated with a novel RPGRIP1 dominant variant. Methods Case report. The patient …
associated with a novel RPGRIP1 dominant variant. Methods Case report. The patient …
Case report: Familial foveal retinoschisis caused by CRB1 gene mutation in a family with recessive inheritance
S Liu, Y Ren, D Wang, D Xiao, Z Li, D Xu, Y Sun… - Frontiers in …, 2023 - frontiersin.org
X-linked retinoschisis is more common in male children and rare in females. Clinically, male
patients mainly present with early onset visual impairment or vision loss, and retinal …
patients mainly present with early onset visual impairment or vision loss, and retinal …
Pigmented paravenous chorioretinal atrophy: A fortuitous finding in a patient with fronto-ethmoidal mucocoele
YO Babalola, AA Ibiyemi - Nigerian Journal of Vitreoretinal …, 2023 - journals.lww.com
A 56-year-old Nigerian male patient presented to the eye clinic with a six-month history of
progressive deterioration of vision in the right eye which was preceded by a one-month …
progressive deterioration of vision in the right eye which was preceded by a one-month …
Macular Neovascularization in a Patient with Pigmented Paravenous Chorioretinal Atrophy.
A 60-year-old male patient admitted to our clinic with complaints of decreased vision,
nyctalopia, and metamorphopsia in both eyes, mainly in the left eye. The best-corrected …
nyctalopia, and metamorphopsia in both eyes, mainly in the left eye. The best-corrected …