Bilateral limbal stem cell deficiency with xeroderma pigmentosum in a young Asian child

KEY CLINICAL MESSAGE: Xeroderma pigmentosum is an autosomal recessive disorder with various ocular manifestations of which bilateral limbal stem cell deficiency is a rare manifestation. Timely diagnosis and meticulous management are vital in these cases to prevent irreversible ocular sequelae. ABSTR...

Descripción completa

Detalles Bibliográficos
Autores principales: Gurnani, Bharat, Kaur, Kirandeep
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Case Images
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10387588/
https://www.ncbi.nlm.nih.gov/pubmed/37529126
http://dx.doi.org/10.1002/ccr3.7746

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10387588/
https://www.ncbi.nlm.nih.gov/pubmed/37529126
http://dx.doi.org/10.1002/ccr3.7746

Ejemplares similares