Literature DB >> 31100171

CRAO in Moyamoya Syndrome Associated With Southampton Hemoglobinopathy.

Jared J Ebert, Robert A Sisk.   

Abstract

The authors present the first case of central retinal artery occlusion (CRAO) resulting from moyamoya syndrome secondary to Southampton hemoglobinopathy. A 12-year-old Hispanic girl with a history of Southampton hemoglobinopathy with moyamoya syndrome presented with amaurosis fugax in her left eye that resolved within hours except for an inferior paracentral scotoma. She had left ophthalmic artery occlusion on magnetic resonance angiogram. Seven months later, spectral-domain optical coherence tomography showed diffuse inner retinal thinning. She was diagnosed with transient CRAO. The authors conclude that CRAO can result from moyamoya syndrome secondary to an underlying hemoglobinopathy. Multimodal imaging demonstrated residual inner retinal injury despite reperfusion. [Ophthalmic Surg Lasers Imaging Retina. 2019;50:e166-e170.]. Copyright 2019, SLACK Incorporated.

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Year:  2019        PMID: 31100171     DOI: 10.3928/23258160-20190503-17

Source DB:  PubMed          Journal:  Ophthalmic Surg Lasers Imaging Retina        ISSN: 2325-8160            Impact factor:   1.300


  3 in total

1.  Central retinal artery occlusion as initial presentation of Moyamoya disease in a middle-aged woman.

Authors:  Alekya P Rajanala; Hong-Gam T Le; Manjot K Gill
Journal:  Am J Ophthalmol Case Rep       Date:  2020-04-10

Review 2.  The rare hemoglobin variant Hb Mizuho: report of a Swiss family and literature review.

Authors:  Linet Njue; Cesare Medri; Peter Keller; Miriam Diepold; Behrouz Mansouri Taleghani; Alicia Rovó
Journal:  Ann Hematol       Date:  2021-02-15       Impact factor: 3.673

Review 3.  Western Moyamoya Phenotype: A Scoping Review.

Authors:  Raphael Miller; Santiago R Unda; Ryan Holland; David J Altschul
Journal:  Cureus       Date:  2021-11-22
  3 in total

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