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...
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| Main Authors: | , , , , , , , , |
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| Other Authors: | |
| Format: | Article |
| Published: |
2020
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| Subjects: | |
| Online Access: | https://repository.li.mahidol.ac.th/handle/123456789/58064 |
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| Institution: | Mahidol University |