Detection of an insertion deletion of region 8q13-q21.2 in a patient with Duane syndrome: implications for mapping and cloning a Duane gene

被引:43
作者
Calabrese, G
Stuppia, L
Morizio, E
Franchi, PG
Pompetti, F
Mingarelli, R
Marsilio, T
Rocchi, M
Gallenga, PE
Palka, G
Dallapiccola, B
机构
[1] Univ G DAnnunzio, Cattedra Genet, Chieti, Italy
[2] Univ G DAnnunzio, Cattedra Oftalmol, Chieti, Italy
[3] Mendel CSS IRCCS, Rome, Italy
[4] Univ Rome Tor Vergata, Cattedra Genet Med, Rome, Italy
[5] Univ Bari, Ist Genet, I-70121 Bari, Italy
关键词
chromosome; 8; deletion; Duane syndrome; mapping; complex rearrangement;
D O I
10.1038/sj.ejhg.5200173
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Duane syndrome (MIM126800) is an autosomal dominant disease responsible for 1% of all strabismus cases and has been related to a 8q12-13 contiguous gene syndrome. We report on an insertion of chromosome region 8q13-q21.2 on to band 6q25 in a patient presenting with Duane syndrome, mental retardation, and other dysmorphisms. FISH analysis using chromosome 8 radiation hybrid LIA2L indicated a concurrent deletion within the go rearranged region. These results were corroborated by STR-PCR analysis and FISH using YAC contig WC8.8 disclosed a deletion in 8q13. Comparison of the two known patients with Duane syndrome associated with deletion of go identifies a small region of overlap (SRO) of < 3 cM extending from D8S533 and D8S1767 in which a Duane syndrome locus is assigned. In addition YAC analysis in our patient showed that go-rearrangement was rather complex since go deletion and insertion occurred in two distinct segments separated by a region which maintained its location on go.
引用
收藏
页码:187 / 193
页数:7
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