RENAL FINDINGS IN 40 INDIVIDUALS WITH WILLIAMS SYNDROME

被引:80
作者
POBER, BR
LACRO, RV
RICE, C
MANDELL, V
TEELE, RL
机构
[1] CHILDRENS HOSP MED CTR, DIV GENET, BOSTON, MA 02115 USA
[2] CHILDRENS HOSP MED CTR, DEPT CARDIOL, BOSTON, MA 02115 USA
[3] CHILDRENS HOSP MED CTR, DEPT RADIOL, BOSTON, MA 02115 USA
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1993年 / 46卷 / 03期
关键词
RENAL ABNORMALITIES; RENAL ARTERY STENOSIS; NEPHROCALCINOSIS;
D O I
10.1002/ajmg.1320460306
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We tabulated the frequency of renal abnormalities in 40 Williams syndrome individuals presenting for medical and/or developmental assessment to a multi-disciplinary Williams syndrome program. The average age at time of assessment was 7 2/12 years. Seven individuals (7/40 = 18%) had abnormalities detected, including nephrocalcinosis = 2; marked asymmetry in kidney size = 2; small kidneys = 1; solitary kidney = 1; and pelvic kidney = 1. Renal function was also assessed. Two individuals had evidence of renal dysfunction, one secondary to nephrocalcinosis and the second due to hypercalcemia and interstitial nephritis of unclear pathogenesis. We examined the frequency of renal artery stenosis in 9 individuals who underwent abdominal angiography during cardiac catheterization. We found unilateral or bilateral mild renal artery narrowing in 4 individuals and normal renal arteries in the remaining 5. Persistent hypertension occurred in only 2 individuals and did not correlate with renal artery status. We conclude that intrinsic renal anomalies, as well as problems secondary to hypercalcemia, occur with sufficient frequency to warrant baseline renal screening in all individuals with Williams syndrome.
引用
收藏
页码:271 / 274
页数:4
相关论文
共 15 条
[1]   SYNDROME OF SUPRAVALVULAR AORTIC STENOSIS PERIPHERAL PULMONARY STENOSIS MENTAL RETARDATION + SIMILAR FACIAL APPEARANCE [J].
BEUREN, AJ ;
APITZ, J ;
EBERLE, P ;
HARMJANZ, D ;
SCHULZE, C .
AMERICAN JOURNAL OF CARDIOLOGY, 1964, 13 (04) :471-&
[2]   RENAL-INSUFFICIENCY IN WILLIAMS SYNDROME [J].
BIESECKER, LG ;
LAXOVA, R ;
FRIEDMAN, A .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1987, 28 (01) :131-135
[3]   INCREASED RENAL MEDULLARY ECHOGENICITY IN PATIENTS WITH WILLIAMS SYNDROME [J].
COTE, G ;
JEQUIER, S ;
KAPLAN, P .
PEDIATRIC RADIOLOGY, 1989, 19 (6-7) :481-483
[4]   SPECTRUM OF RENAL ANOMALIES IN PATIENTS WITH WILLIAMS SYNDROME [J].
INGELFINGER, JR ;
NEWBURGER, JW .
JOURNAL OF PEDIATRICS, 1991, 119 (05) :771-773
[5]   PROGRESSIVE VASCULAR-LESIONS IN WILLIAMS-BEUREN SYNDROME [J].
INO, T ;
NISHIMOTO, K ;
IWAHARA, M ;
AKIMOTO, K ;
BOKU, H ;
KANEKO, K ;
TOKITA, A ;
YABUTA, K ;
TANAKA, J .
PEDIATRIC CARDIOLOGY, 1988, 9 (01) :55-58
[6]   WILLIAMS ELFIN FACIES SYNDROME - NEW PERSPECTIVE [J].
JONES, KL ;
SMITH, DW .
JOURNAL OF PEDIATRICS, 1975, 86 (05) :718-723
[7]  
KAPLAN P, 1989, PEDIATRICS, V84, P895
[8]  
LACRO RV, 1992, IN PRESS P GREENWOOD
[9]   IDIOPATHIC INFANTILE HYPERCALCEMIA - A CONTINUING ENIGMA [J].
MARTIN, NDT ;
SNODGRASS, GJAI ;
COHEN, RD .
ARCHIVES OF DISEASE IN CHILDHOOD, 1984, 59 (07) :605-613
[10]   NATURAL-HISTORY OF WILLIAMS SYNDROME - PHYSICAL CHARACTERISTICS [J].
MORRIS, CA ;
DEMSEY, SA ;
LEONARD, CO ;
DILTS, C ;
BLACKBURN, BL .
JOURNAL OF PEDIATRICS, 1988, 113 (02) :318-326