APPARENT POSTNATAL ONSET OF SOME MANIFESTATIONS OF THE WIEDEMANN-BECKWITH SYNDROME

被引:27
作者
CHITAYAT, D
ROTHCHILD, A
LING, E
FRIEDMAN, JM
COUCH, RM
YONG, SL
BALDWIN, VJ
HALL, JG
机构
[1] UNIV BRITISH COLUMBIA,VANCOUVER V6T 1W5,BC,CANADA
[2] BRITISH COLUMBIA CHILDRENS HOSP,DEPT MED GENET,VANCOUVER,BC,CANADA
[3] BRITISH COLUMBIA CHILDRENS HOSP,DEPT PATHOL,VANCOUVER,BC,CANADA
[4] BRITISH COLUMBIA CHILDRENS HOSP,METAB INVEST UNIT,VANCOUVER,BC,CANADA
[5] BRITISH COLUMBIA CHILDRENS HOSP,SPECIAL CARE NURSERY,VANCOUVER,BC,CANADA
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1990年 / 36卷 / 04期
关键词
hypoglycemia; macroglossia; nephromegaly; placenta; umbilical hernia;
D O I
10.1002/ajmg.1320360412
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report on 2 patients who were apparently normal at birth but later developed characteristics of Wiedemann-Beckwith syndrome (WBS). Both had hypoglycemia neonatally and gradually developed coarse facial changes, umbilical hernia, and macroglossia. Renal sonography done after the macroglossia developed showed large kidneys in both. The placentas were carefully examined in both cases but findings described as typical of WBS were only found in one. The clinical evolution of these infants suggests that some WBS manifestations may have their onset postnatally in some cases. We postulate that the cellular hyperplasia and hypertrophy characteristic of WBS may be caused by persistent rests of embryonal cells that secrete paracrine and/or endocrine growth factors.
引用
收藏
页码:434 / 439
页数:6
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