Optical coherence tomography findings in three patients with Werner syndrome

BACKGROUND: Werner syndrome is a rare, autosomal recessive disorder characterised by premature aging. It is a typical hereditary progeroid syndrome that can be difficult to diagnose owing to its rarity and the similarity of some of its symptoms, such as juvenile cataracts, to other common ophthalmol...

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Detalles Bibliográficos
Autores principales: Nagai, Tatsuya, Yokouchi, Hirotaka, Miura, Gen, Koshizaka, Masaya, Maezawa, Yoshiro, Oshitari, Toshiyuki, Yokote, Koutaro, Baba, Takayuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9675230/
https://www.ncbi.nlm.nih.gov/pubmed/36403005
http://dx.doi.org/10.1186/s12886-022-02660-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9675230/
https://www.ncbi.nlm.nih.gov/pubmed/36403005
http://dx.doi.org/10.1186/s12886-022-02660-z

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