Literature DB >> 18620881

Morning glory disk anomaly with ipsilateral capillary hemangioma, agenesis of the internal carotid artery, and Horner syndrome: a variant of PHACES syndrome?

Narman Puvanachandra1, Manraj K Heran, Christopher J Lyons.   

Abstract

We describe a 6-week-old girl with a right upper lid capillary hemangioma, ipsilateral morning glory disk anomaly, microphthalmos, Mittendorf dot, and Horner syndrome. The ipsilateral internal carotid artery was also found to be absent. To our knowledge, this is the first patient to be reported with this group of findings. We suggest that this represents an overlap between morning glory disk and intracranial vascular abnormalities, a recognized association, and PHACES syndrome (posterior fossa malformations, hemangiomas, arterial anomalies, cardiac defects, eye, and sternal abnormalities). We discuss the common embryological basis for these abnormalities, which point to a widespread but highly variable disorder of mesodermal differentiation.

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Year:  2008        PMID: 18620881     DOI: 10.1016/j.jaapos.2008.04.005

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


  3 in total

Review 1.  Imaging of Horner syndrome in pediatrics: association with neuroblastoma.

Authors:  Hedieh Khalatbari; Gisele E Ishak
Journal:  Pediatr Radiol       Date:  2020-10-06

2.  Morning glory disc anomaly: characteristic MR imaging findings.

Authors:  S Ellika; C D Robson; G Heidary; M J Paldino
Journal:  AJNR Am J Neuroradiol       Date:  2013-05-09       Impact factor: 3.825

3.  PHACE(S) syndrome: Report of a case with new ocular and systemic manifestations.

Authors:  Raheleh Assari; Vahid Ziaee; Sasan Moghimi; Mohammad Reza Akbari; Arash Mirmohammadsadeghi
Journal:  J Curr Ophthalmol       Date:  2016-12-27
  3 in total

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