Coats plus syndrome: a rare cause of severe gastrointestinal tract bleeding in children - a case report
Abstract Background Coats plus syndrome, cerebroretinal microangiopathy with calcifications and cysts, is a rare disease with autosomal recessive pattern occurring due to a mutation in CTC1, encoding conserved telomere maintenance component 1, gene. Besides retinal involvement, abnormalities in brai...
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| Main Authors: | , , , , , |
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| Format: | Book |
| Published: |
BMC,
2022-03-01T00:00:00Z.
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| Subjects: | |
| Online Access: | Connect to this object online. |
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