Literature DB >> 28376043

MULTIMODAL IMAGING OF MOSAIC RETINOPATHY IN CARRIERS OF HEREDITARY X-LINKED RECESSIVE DISEASES.

An-Lun Wu1, Jung-Pan Wang2,3, Yun-Ju Tseng4, Laura Liu1,5, Yu-Chuan Kang1, Kuan-Jen Chen1,5, An-Ning Chao1,5, Lung-Kun Yeh1,5, Tun-Lu Chen1,5, Yih-Shiou Hwang1,5, Wei-Chi Wu1,5, Chi-Chun Lai1,5, Nan-Kai Wang1,5.   

Abstract

PURPOSE: To investigate the clinical features in carriers of X-linked retinitis pigmentosa, X-linked ocular albinism, and choroideremia (CHM) using multimodal imaging and to assess their diagnostic value in these three mosaic retinopathies.
METHODS: We prospectively examined 14 carriers of 3 X-linked recessive disorders (X-linked retinitis pigmentosa, X-linked ocular albinism, and CHM). Details of abnormalities of retinal morphology were evaluated using fundus photography, fundus autofluorescence (FAF) imaging, and spectral domain optical coherence tomography.
RESULTS: In six X-linked retinitis pigmentosa carriers, fundus appearance varied from unremarkable to the presence of tapetal-like reflex and pigmentary changes. On FAF imaging, all carriers exhibited a bright radial reflex against a dark background. By spectral domain optical coherence tomography, loss of the ellipsoid zone in the macula was observed in 3 carriers (50%). Regarding the retinal laminar architecture, 4 carriers (66.7%) showed thinning of the outer nuclear layer and a dentate appearance of the outer plexiform layer. All five X-linked ocular albinism carriers showed a characteristic mud-splatter patterned fundus, dark radial streaks against a bright background on FAF imaging, and a normal-appearing retinal structure by spectral domain optical coherence tomography imaging. Two of the 3 CHM carriers (66.7%) showed a diffuse moth-eaten appearance of the fundus, and all 3 showed irregular hyper-FAF and hypo-FAF spots throughout the affected area. In the CHM carriers, the structural changes observed by spectral domain optical coherence tomography imaging were variable.
CONCLUSION: Our findings in an Asian cohort suggest that FAF imaging is a practical diagnostic test for differentiating X-linked retinitis pigmentosa, X-linked ocular albinism, and CHM carriers. Wide-field FAF is an easy and helpful adjunct to testing for the correct diagnosis and identification of lyonization in carriers of these three mosaic retinopathies.

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Year:  2018        PMID: 28376043     DOI: 10.1097/IAE.0000000000001629

Source DB:  PubMed          Journal:  Retina        ISSN: 0275-004X            Impact factor:   4.256


  2 in total

1.  Prospective Study of the Phenotypic and Mutational Spectrum of Ocular Albinism and Oculocutaneous Albinism.

Authors:  Hwei Wuen Chan; Elena R Schiff; Vijay K Tailor; Samantha Malka; Magella M Neveu; Maria Theodorou; Mariya Moosajee
Journal:  Genes (Basel)       Date:  2021-03-30       Impact factor: 4.096

2.  Clinical Manifestations and Genetic Analysis of 5 Korean Choroideremia Patients Initially Diagnosed With Retinitis Pigmentosa.

Authors:  Jin Ha Kim; Jung Woo Han; Eun Woo Choi; Ji Hong Bang; Hee Jeong Shin; Mi-Ae Jang; Jong-Young Lee; Jeong Nam Choi; Hun Soo Chang; Tae Kwann Park
Journal:  J Korean Med Sci       Date:  2022-01-17       Impact factor: 2.153

  2 in total

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