Small extra ring chromosome derived from chromosome 10p: Clinical report and characterisation by FISH

被引:27
作者
Blennow, E
Tillberg, E
机构
[1] KAROLINSKA INST,DEPT MOLEC MED,STOCKHOLM,SWEDEN
[2] KS ST GORAN HOSP,DEPT PEDIAT,STOCKHOLM,SWEDEN
关键词
extra ring chromosome; fluorescence in situ hybridisation; chromosome; 10;
D O I
10.1136/jmg.33.5.399
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We present a case with a small extra ring chromosome which was found in 66% of lymphocytes on routine cytogenetic examination. FISH analyses, using centromere specific and single copy probes, showed that the extra ring chromosome was derived from the most proximal part of 10p, close to the centromere. The patient has a unilateral cleft lip and palate, mild dysmorphic features, and mild mental retardation. Only a limited number of extra ring chromosomes have been characterised so far. To our knowledge, this is the first reported patient with an extra ring chromosome derived from chromosome 10p.
引用
收藏
页码:399 / 402
页数:4
相关论文
共 30 条
[21]   CHROMOSOME-ABNORMALITIES FOUND AMONG 34910 NEWBORN CHILDREN - RESULTS FROM A 13-YEAR INCIDENCE STUDY IN ARHUS, DENMARK [J].
NIELSEN, J ;
WOHLERT, M .
HUMAN GENETICS, 1991, 87 (01) :81-83
[22]  
PLATTNER R, 1993, HUM GENET, V91, P589
[23]   UNIPARENTAL DISOMY EXPLAINS THE OCCURRENCE OF THE ANGELMAN OR PRADER-WILLI-SYNDROME IN PATIENTS WITH AN ADDITIONAL SMALL INV DUP(15) CHROMOSOME [J].
ROBINSON, WP ;
WAGSTAFF, J ;
BERNASCONI, F ;
BACCICHETTI, C ;
ARTIFONI, L ;
FRANZONI, E ;
SUSLAK, L ;
SHIH, LY ;
AVIV, H ;
SCHINZEL, AA .
JOURNAL OF MEDICAL GENETICS, 1993, 30 (09) :756-760
[24]   MARKER CHROMOSOMES IN A SERIES OF 10000 PRENATAL DIAGNOSES - CYTOGENETIC AND FOLLOW-UP-STUDIES [J].
SACHS, ES ;
VANHEMEL, JO ;
DENHOLLANDER, JC ;
JAHODA, MGJ .
PRENATAL DIAGNOSIS, 1987, 7 (02) :81-89
[25]  
SILAHTAROGLU AN, 1995, CLIN GENET, V47, P270
[26]  
TEMPLE K, 1995, NAT GENET, V9, P110
[27]   OUTCOME OF CASES OF DENOVO STRUCTURAL REARRANGEMENTS DIAGNOSED AT AMNIOCENTESIS [J].
WARBURTON, D .
PRENATAL DIAGNOSIS, 1984, 4 :69-80
[28]  
WARBURTON D, 1991, AM J HUM GENET, V49, P995
[29]   CHARACTERIZATION OF A DE NOVO 48,XX, + R(X), + R(17) BY INSITU HYBRIDIZATION IN A PATIENT WITH NEUROFIBROMATOSIS (NF1) [J].
WIKTOR, A ;
VANDYKE, DL ;
WEISS, L .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1993, 45 (01) :22-24
[30]   DEVELOPMENT OF 124 SEQUENCE-TAGGED SITES AND CYTOGENETIC LOCALIZATION OF 217 COSMIDS FOR HUMAN-CHROMOSOME-10 [J].
ZHENG, CJ ;
MA, NSF ;
DORMAN, TE ;
WANG, MT ;
BRAUNSCHWEIGER, K ;
SOARES, L ;
SCHUSTER, MK ;
ROTHSCHILD, CB ;
BOWDEN, DW ;
TORREY, D ;
KEITH, TP ;
MOIR, DT ;
MAO, JI .
GENOMICS, 1994, 22 (01) :55-67