Gelatinous drop-like corneal dystrophy with a novel mutation of TACSTD2 manifested in combination with spheroidal degeneration in a Chinese patient

PURPOSE: To report the clinicopathological findings of a Chinese patient with an unusual phenotype of gelatinous drop-like corneal dystrophy (GDLD) combined with spheroidal degeneration and to detect molecular defect in the tumor-associated calcium signal transducer 2 (TACSTD2) gene. METHODS: Extens...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Bei, Yao, Yu-Feng
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2927379/
https://www.ncbi.nlm.nih.gov/pubmed/20806038

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2927379/
https://www.ncbi.nlm.nih.gov/pubmed/20806038

Ejemplares similares