DUCHENNE MUSCULAR-DYSTROPHY - NEGATIVE ELECTRORETINOGRAMS AND NORMAL DARK-ADAPTATION - REAPPRAISAL OF ASSIGNMENT OF X-LINKED INCOMPLETE CONGENITAL STATIONARY NIGHT BLINDNESS

被引:27
作者
JENSEN, H
WARBURG, M
SJO, O
SCHWARTZ, M
机构
[1] UNIV COPENHAGEN, GENTOFTE HOSP, DIV PAEDIAT OPHTHALMOL & HANDICAPS, DK-2820 GENTOFTE, DENMARK
[2] RIGSHOSP, DEPT PAEDIAT, CLIN GENET SECT, COPENHAGEN, DENMARK
关键词
D O I
10.1136/jmg.32.5.348
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Aland Island eye disease (AIED) and X linked congenital stationary night blindness (CSNB) have been mapped to Xp11.3. Patients have been described with deletions of the Duchenne muscular dystrophy (DMD) gene who also had a negative electroretinogram (ERG) similar to that seen in patients with CSNB and AIED. This seems to confirm that some cases of AIED and CSNB map to Xp21. We examined 16 boys with DMD/BMD (Pecker muscular dystrophy) of whom 10 had negative ERGs, eight of them having deletions downstream from exon 44. Normal dark adaptation thresholds were observed in all patients and there were no anomalous visual functions. Hence, CSNB cannot be assigned to Xp21 and negative ERG in DMD/BMD is not associated with eye disease. Six boys with DR DMD/BMD had normal ERGs. We speculate that a retinal or glial dystrophin may be truncated or absent in the boys with negative ERGs.
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页码:348 / 351
页数:4
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