| Autor: |
Torii, Kaoruko, Nishina, Sachiko, Morikawa, Hazuki, Mizobuchi, Kei, Takayama, Masakazu, Tachibana, Nobutaka, Kurata, Kentaro, Hikoya, Akiko, Sato, Miho, Nakano, Tadashi, Fukami, Maki, Azuma, Noriyuki, Hayashi, Takaaki, Saitsu, Hirotomo, Hotta, Yoshihiro |
| Předmět: |
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| Zdroj: |
International Journal of Molecular Sciences; Sep2023, Vol. 24 Issue 18, p13678, 15p |
| Abstrakt: |
Leber congenital amaurosis (LCA) is the most severe form of inherited retinal dystrophy. RPGRIP1-related LCA accounts for 5–6% of LCA. We performed whole-exome sequencing and whole-genome sequencing (WGS) on 29 patients with clinically suspected LCA and examined ophthalmic findings in patients with biallelic pathogenic variants of RPGRIP1. In addition to five previously reported cases, we identified five cases from four families with compound heterozygous RPGRIP1 variants using WGS. Five patients had null variants comprising frameshift variants, an Alu insertion, and microdeletions. A previously reported 1339 bp deletion involving exon 18 was found in four cases, and the deletion was relatively prevalent in the Japanese population (allele frequency: 0.002). Microdeletions involving exon 1 were detected in four cases. In patients with RPGRIP1 variants, visual acuity remained low, ranging from light perception to 0.2, and showed no correlation with age. In optical coherence tomography images, the ellipsoid zone (EZ) length decreased with age in all but one case of unimpaired EZ. The retinal structure was relatively preserved in all cases; however, there were cases with great differences in visual function compared to their siblings and a 56-year-old patient who still had a faint EZ line. Structural abnormalities may be important genetic causes of RPGRIP1-related retinal dystrophy in Japanese patients, and WGS was useful for detecting them. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
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