Identification of Pathogenic Variants in the CHM Gene in Two Korean Patients With Choroideremia
Annals of Laboratory Medicine
; : 438-442, 2017.
Article
en En
| WPRIM
| ID: wpr-168471
Biblioteca responsable:
WPRO
ABSTRACT
Choroideremia is a rare X-linked disorder causing progressive chorioretinal atrophy. Affected patients develop night blindness with progressive peripheral vision loss and eventual blindness. Herein, we report two Korean families with choroideremia. Multimodal imaging studies showed that the probands had progressive loss of visual field with characteristic chorioretinal atrophy, while electroretinography demonstrated nearly extinguished cone and rod responses compatible with choroideremia. Sanger sequencing of all coding exons and flanking intronic regions of the CHM gene revealed a novel small deletion at a splice site (c.184_189+3delTACCAGGTA) in one patient and a deletion of the entire exon 9 in the other. This is the first report on a molecular genetic diagnosis of choroideremia in Korean individuals. Molecular diagnosis of choroideremia should be widely adopted for proper diagnosis and the development of new treatment modalities including gene therapy.
Palabras clave
Texto completo:
1
Base de datos:
WPRIM
Asunto principal:
Atrofia
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Intrones
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Terapia Genética
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Campos Visuales
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Coroideremia
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Ceguera
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Ceguera Nocturna
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Exones
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Diagnóstico
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Electrorretinografía
Tipo de estudio:
Diagnostic_studies
/
Prognostic_studies
Límite:
Humans
Idioma:
En
Revista:
Annals of Laboratory Medicine
Año:
2017
Tipo del documento:
Article