Bilateral Retinal Detachment after prophylactic laser therapy in Knobloch Syndrome.

PURPOSE: Knobloch Syndrome (COL18A1-related) is a rare inherited vitreoretinopathy characterized by early-onset high myopia, regmatogenous retinal detachment and occipital skull and cutaneous defects. Although prophylactic retinal procedures have been proposed for related vitreoretinopathies, data supporting their use in Knobloch syndrome is scarce. METHODS: Case Report. RESULTS: An 8-year-old girl with genetically confirmed Knobloch syndrome who developed bilateral rhegmatogenous retinal detachment seven days after prophylactic laser therapy performed in a single-session bilaterally. Ultrawide-field retinography revealed bilateral inferotemporal retinal detachment associated with peripheral punched-out lesions. The patient underwent prompt sequential scleral buckle surgery with cryopexy and subretinal fluid drainage as indicated. Both retinas were successfully reattached and visual acuity returned to baseline values in the early postoperative period. CONCLUSION: This case highlights limited evidence supporting laser prophylaxis in Knobloch syndrome and the importance of cautious, individualized decision-making as well as the need for further research to recommend for or against prophylaxis in this syndrome.

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Publication Details

Journal
Retinal Cases & Brief Reports
Published
2026-10-15
DOI
https://doi.org/10.1097/icb.0000000000002005
Primary Topic
Retinal and Macular Surgery
Type
article
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article

Bilateral Retinal Detachment after prophylactic laser therapy in Knobloch Syndrome.

Maria Frasson, Márcio Bittar Nehemy, Brunelle Francino Nunes, Joziele S. Lima et al.
Retinal Cases & Brief Reports
Retinal and Macular Surgery
article

Bilateral Retinal Detachment after prophylactic laser therapy in Knobloch Syndrome.

Maria Frasson, Márcio Bittar Nehemy, Brunelle Francino Nunes, Joziele S. Lima, Caio A. Silva
article en

Abstract

PURPOSE: Knobloch Syndrome (COL18A1-related) is a rare inherited vitreoretinopathy characterized by early-onset high myopia, regmatogenous retinal detachment and occipital skull and cutaneous defects. Although prophylactic retinal procedures have been proposed for related vitreoretinopathies, data supporting their use in Knobloch syndrome is scarce. METHODS: Case Report. RESULTS: An 8-year-old girl with genetically confirmed Knobloch syndrome who developed bilateral rhegmatogenous retinal detachment seven days after prophylactic laser therapy performed in a single-session bilaterally. Ultrawide-field retinography revealed bilateral inferotemporal retinal detachment associated with peripheral punched-out lesions. The patient underwent prompt sequential scleral buckle surgery with cryopexy and subretinal fluid drainage as indicated. Both retinas were successfully reattached and visual acuity returned to baseline values in the early postoperative period. CONCLUSION: This case highlights limited evidence supporting laser prophylaxis in Knobloch syndrome and the importance of cautious, individualized decision-making as well as the need for further research to recommend for or against prophylaxis in this syndrome.

Retinal Cases & Brief Reports
Universidade Federal de Minas Gerais (BR)
Good health and well-being
Openalex Percentile: Top 13%
Retinal and Macular Surgery
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