Literature DB >> 28864049

Cerebroretinal microangiopathy with calcifications and cysts (CRMCC) or "Coats Plus": when peripheral retinal vasculature signals neurologic disease.

Sasha Mansukhani1, Mai Lan Ho2, Ralitza H Gavrilova3, Brian G Mohney1, Polly A Quiram4, Michael C Brodsky5.   

Abstract

An 8-month-old girl presented with vitreous hemorrhage, peripheral retinal arteriovenous anastomosis, and hypoplasia of the thumb. Magnetic resonance imaging of the brain showed multiple hyperintensities, cysts, and calcifications in the white matter. DNA testing showed a mutation in one allele of the CTC gene, supporting the diagnosis of cerebroretinal microangiopathy with calcifications and cysts (CRMCC), or Coats plus disease, despite which designation this condition can present without subretinal exudate. In infants with peripheral retinal vascular disease, neuroimaging can identify the characteristic abnormalities of CRMCC.
Copyright © 2017 American Association for Pediatric Ophthalmology and Strabismus. Published by Elsevier Inc. All rights reserved.

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Year:  2017        PMID: 28864049     DOI: 10.1016/j.jaapos.2017.04.015

Source DB:  PubMed          Journal:  J AAPOS        ISSN: 1091-8531            Impact factor:   1.220


  2 in total

1.  CTC1 mutations in a Brazilian family with progeroid features and recurrent bone fractures.

Authors:  Forough Sargolzaeiaval; Jiaming Zhang; Jennifer Schleit; Davor Lessel; Christian Kubisch; Debora R Precioso; David Sillence; Fuki M Hisama; Michael Dorschner; George M Martin; Junko Oshima
Journal:  Mol Genet Genomic Med       Date:  2018-11-04       Impact factor: 2.183

2.  Coats plus syndrome: a rare cause of severe gastrointestinal tract bleeding in children - a case report.

Authors:  Selcen Bozkurt; Ayse Merve Usta; Nafiye Urganci; Nida Gulderen Kalay; Gulsen Kose; Evrim Ozmen
Journal:  BMC Pediatr       Date:  2022-03-08       Impact factor: 2.125

  2 in total

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