Diagnosis of Fanconi anemia in patients without congenital malformations: An international Fanconi anemia registry study

被引:0
作者
Giampietro, PF
Verlander, PC
Davis, JG
Auerbach, AD
机构
[1] ROCKEFELLER UNIV,LAB HUMAN GENET & HEMATOL,NEW YORK,NY 10021
[2] CORNELL UNIV,NEW YORK HOSP,COLL MED,DIV HUMAN GENET,NEW YORK,NY
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1997年 / 68卷 / 01期
关键词
Fanconi anemia; minor congenital anomalies; microphthalmia; short stature; skin pigmentation abnormalities;
D O I
10.1002/(SICI)1096-8628(19970110)68:1<58::AID-AJMG11>3.3.CO;2-K
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Data were analyzed from 419 Fanconi anemia (FA) patients enrolled in the American Registry of the International Fanconi Anemia Registry (IFAR) to determine whether Fanconi anemia (FA) patients without major congenital malformations (CM) have distinguishing characteristics that can lead to an earlier diagnosis, These included 377 patients reported by physicians to the IFAR and 42 patients examined by us, The number of FA patients in each group without CM was 128 and 16, respectively; one third of all patients lacked CM, We found that height, weight, and head circumference were less than or equal to 5th centile in 26.6%, 18.0%, and 8.6% of FA patients without CM referred to the IFAR, and in 43.8%, 25.0%, and 43.8% of FA patients without CM examined by us, Minor anomalies were reported in 9.4% of FA patients without CM referred to the IFAR and 100% of FA patients without CM examined by us, Most FA patients without CM have alterations in growth parameters, skin pigmentation abnormalities, or microphthalmia, Increased awareness of the complete spectrum of FA by clinicians will enable an earlier diagnosis to be made. (C) 1997 Wiley-Liss, Inc.
引用
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页码:58 / 61
页数:4
相关论文
共 16 条
[1]  
AUERBACH AD, 1981, PEDIATRICS, V67, P128
[2]  
AUERBACH AD, 1989, BLOOD, V73, P391
[3]  
AUERBACH AD, 1993, EXP HEMATOL, V21, P731
[4]   HEMATOLOGIC ABNORMALITIES IN FANCONI-ANEMIA - AN INTERNATIONAL FANCONI-ANEMIA REGISTRY STUDY [J].
BUTTURINI, A ;
GALE, RP ;
VERLANDER, PC ;
ADLERBRECHER, B ;
GILLIO, AP ;
AUERBACH, AD .
BLOOD, 1994, 84 (05) :1650-1655
[5]  
Fanconi G, 1927, JB KINDERHEILK, V117, P257
[6]  
GIAMPIETRO PF, 1993, PEDIATRICS, V91, P1116
[7]   HEMATOPOIETIC RECONSTITUTION IN A PATIENT WITH FANCONIS ANEMIA BY MEANS OF UMBILICAL-CORD BLOOD FROM AN HLA-IDENTICAL SIBLING [J].
GLUCKMAN, E ;
BROXMEYER, HE ;
AUERBACH, AD ;
FRIEDMAN, HS ;
DOUGLAS, GW ;
DEVERGIE, A ;
ESPEROU, H ;
THIERRY, D ;
SOCIE, G ;
LEHN, P ;
COOPER, S ;
ENGLISH, D ;
KURTZBERG, J ;
BARD, J ;
BOYSE, EA .
NEW ENGLAND JOURNAL OF MEDICINE, 1989, 321 (17) :1174-1178
[8]  
GLUCKMAN E, 1995, BLOOD, V86, P2856
[9]   CLASSIFICATION OF FANCONI-ANEMIA PATIENTS BY COMPLEMENTATION ANALYSIS - EVIDENCE FOR A 5TH GENETIC SUBTYPE [J].
JOENJE, H ;
LO TEN FOE, JR ;
OOSTRA, AB ;
VANBERKEL, CGN ;
ROOIMANS, MA ;
SCHROEDERKURTH, T ;
WEGNER, RD ;
GILLE, JJP ;
BUCHWALD, M ;
ARWERT, F .
BLOOD, 1995, 86 (06) :2156-2160
[10]  
JONES KL, 1991, SMITHS RECOGNIZABLE, P662