Lens opacities in Bloom syndrome: Case report and review of the literature

被引:8
作者
Cefle, Kivanc [1 ]
Ozturk, Sukru
Gozum, Nilufer
Duman, Nilgun
Mantar, Ferhan
Guler, Kerim
Palanduz, Sukru
机构
[1] Istanbul Univ, Istanbul Fac Med, Dept Internal Med, Div Med Genet, TR-34093 Istanbul, Turkey
[2] Istanbul Univ, Istanbul Fac Med, Dept Ophthalmol, Istanbul, Turkey
[3] Istanbul Samatya Social Secur Hosp, Istanbul, Turkey
[4] Istanbul Univ, Istanbul Fac Med, Dept Internal Med, Emergency Unit, Istanbul, Turkey
关键词
Bloom syndrome; lens; cataract;
D O I
10.1080/13816810701389685
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Bloom syndrome is an autosomal recessive disorder characterized by proportionate short stature, photosensitivity, immunodeficiency, hypogonadism and a tendency to develop various malignancies. The greatly increased frequency of sister chromatid exchanges (reciprocal exchange of homologous segments between the two sister chromatids of a chromosome) is regarded as pathognomonic for BS. We describe an 18-year old girl who presented with short stature. She was diagnosed with BS based on an extremely increased frequency of sister chromatid exchanges. Ophthalmological examination revealed mild lens opacities bilaterally, which, to our knowledge, has not been previously reported to be associated with BS.
引用
收藏
页码:175 / 178
页数:4
相关论文
共 26 条
[1]  
Antonio J R, 1990, Rev Paul Med, V108, P9
[2]   Early-onset drusen in a girl with bloom syndrome:: Probable clinical importance of an ocular manifestation [J].
Aslan, D ;
Öztürk, G ;
Kaya, Z ;
Bideci, A ;
Özdogaan, S ;
Gürsel, T .
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2004, 26 (04) :256-257
[3]   Bloom syndrome: multiple retinopathies in a chromosome breakage disorder [J].
Bhisitkul, RB ;
Rizen, M .
BRITISH JOURNAL OF OPHTHALMOLOGY, 2004, 88 (03) :354-357
[4]   CONGENITAL TELANGIECTATIC ERYTHEMA RESEMBLING LUPUS ERYTHEMATOSUS IN DWARFS - PROBABLY A SYNDROME ENTITY [J].
BLOOM, D .
AMA AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1954, 88 (06) :754-758
[5]   Successful pregnancy in a woman with Bloom syndrome [J].
Chisholm, CA ;
Bray, MJ ;
Karns, LB .
AMERICAN JOURNAL OF MEDICAL GENETICS, 2001, 102 (02) :136-138
[6]  
Colitz Carmen Maria Helena, 2005, International Ophthalmology Clinics, V45, P141
[7]   Ocular manifestations in the inherited DNA repair disorders [J].
Dollfus, H ;
Porto, F ;
Caussade, P ;
Speeg-Schatz, C ;
Sahel, J ;
Grosshans, E ;
Flament, J ;
Sarasin, A .
SURVEY OF OPHTHALMOLOGY, 2003, 48 (01) :107-122
[8]   THE BLOOMS-SYNDROME GENE-PRODUCT IS HOMOLOGOUS TO RECQ HELICASES [J].
ELLIS, NA ;
GRODEN, J ;
YE, TZ ;
STRAUGHEN, J ;
LENNON, DJ ;
CIOCCI, S ;
PROYTCHEVA, M ;
GERMAN, J .
CELL, 1995, 83 (04) :655-666
[9]  
Fryns JP, 1999, GENET COUNSEL, V10, P395
[10]  
GERMAN J, 1989, CLIN GENET, V35, P57