A unique case of coats plus syndrome and dyskeratosis congenita in a patient with CTC1 mutations

A unique case of coats plus syndrome and dyskeratosis congenita in a patient with CTC1 mutations

© 2020, © 2020 Taylor & Francis Group, LLC. Coats plus syndrome (CP) is a rare condition characterized by bilateral exudative retinal telangiectasias with associated systemic disorders primarily affecting the brain, bone and gastrointestinal tract due to a mutation in the CTC1 gene. CTC1 mutat...

Full description

Saved in:
Bibliographic Details
Main Authors: Elaine Han, Nimesh A. Patel, Nicolas A. Yannuzzi, Diana M. Laura, Kenneth C. Fan, Catherin I. Negron, Supalert Prakhunhungsit, Willa L. Thorson, Audina M. Berrocal
Other Authors: University of Miami Leonard M. Miller School of Medicine
Format: Article
Published: 2020
Subjects:
Medicine
Online Access:https://repository.li.mahidol.ac.th/handle/123456789/58064
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Mahidol University

Internet

https://repository.li.mahidol.ac.th/handle/123456789/58064

Similar Items