Cargando…
Coats plus syndrome: a rare cause of severe gastrointestinal tract bleeding in children – a case report
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 brain and os...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8903628/ https://www.ncbi.nlm.nih.gov/pubmed/35260125 http://dx.doi.org/10.1186/s12887-022-03140-5 |