A Prospective Audit Comparing Optos Widefield Imaging to Fundus Examination for Von Hippel-Lindau Retinal Screening

Background Von Hippel-Lindau (VHL) disease is an autosomal dominant multisystem disorder caused by germline mutations at chromosome 3p25-26 in the VHLtumour suppressor gene. Retinal manifestations include capillary haemangiomas that develop in up to 80% of gene carriers. Lifelong retinal surveillanc...

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Detalles Bibliográficos
Autores principales: Iqbal, Naeem, Stahl, Matthew, Lim, Ernest, Al-Khuzaei, Saoud, Jones, Rebecca, Halliday, Dorothy, Downes, Susan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9794529/
https://www.ncbi.nlm.nih.gov/pubmed/36582420
http://dx.doi.org/10.7759/cureus.32814

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9794529/
https://www.ncbi.nlm.nih.gov/pubmed/36582420
http://dx.doi.org/10.7759/cureus.32814

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