Multisystem study of 20 older adults with Williams syndrome

被引:185
作者
Cherniske, EM
Carpenter, TO
Klaiman, C
Young, E
Bregman, J
Insogna, K
Schultz, RT
Pober, BR
机构
[1] Childrens Hosp, Dept Surg, Boston, MA 02115 USA
[2] Massachusetts Gen Hosp Children, Dept Pediat, Boston, MA USA
[3] Yale Sch Med, Ctr Child Study, New Haven, CT USA
[4] Yale Sch Med, Dept Pediat, New Haven, CT USA
[5] Yale Sch Med, Dept Otolaryngol, New Haven, CT USA
[6] Yale Sch Med, Dept Internal Med, New Haven, CT USA
关键词
Williams syndrome; adults; diabetes; hearing loss; diverticulitis; obesity; hypercalcemia; bone density; anxiety; aging;
D O I
10.1002/ajmg.a.30400
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
To address the natural history of Williams syndrome (WS), we performed multisystem assessments on 20 adults with WS over 30 years of age and documented a high frequency of problems in multiple organ systems. The most striking and consistent findings were: abnormal body habitus; mild-moderate high frequency sensorineural hearing loss; cardiovascular disease and hypertension; gastrointestinal symptoms including diverticular disease; diabetes and abnormal glucose tolerance on standard oral glucose tolerance testing; subclinical hypothyroidism; decreased bone mineral density on DEXA scanning; and a high frequency of psychiatric symptoms, most notably anxiety, often requiring multimodal therapy. Review of brain MRI scans did not demonstrate consistent pathology. The adults in our cohort were not living independently and the vast majority were not competitively employed. Our preliminary findings raise concern about the occurrence of mild accelerated aging, which may additionally complicate the long-term natural history of older adults with WS. We provide monitoring guidelines to assist in the comprehensive care of adults with WS. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:255 / 264
页数:10
相关论文
共 64 条
[1]  
*AM AC PED COMM GE, 2001, PEDIATRICS, V107, P1192
[2]   RENAL-INSUFFICIENCY IN WILLIAMS SYNDROME [J].
BIESECKER, LG ;
LAXOVA, R ;
FRIEDMAN, A .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1987, 28 (01) :131-135
[3]  
BRADLEY EA, 1989, J MENT DEFIC RES, V33, P175
[4]  
Broder K, 1999, AM J MED GENET, V83, P356, DOI 10.1002/(SICI)1096-8628(19990423)83:5<356::AID-AJMG2>3.0.CO
[5]  
2-X
[6]   RADIOULNAR SYNOSTOSIS IN WILLIAMS-SYNDROME - A HISTORICAL OVERVIEW [J].
BZDUCH, V .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1994, 50 (04) :386-386
[7]   NOCTURNAL HYPERPARATHYROIDISM - A FREQUENT FEATURE OF X-LINKED HYPOPHOSPHATEMIA [J].
CARPENTER, TO ;
MITNICK, MA ;
ELLISON, A ;
SMITH, C ;
INSOGNA, KL .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 78 (06) :1378-1383
[8]   TFII-I, A candidate gene for Williams syndrome cognitive profile: Parallels between regional expression in mouse brain and human phenotype [J].
Danoff, SK ;
Taylor, HE ;
Blackshaw, S ;
Desiderio, S .
NEUROSCIENCE, 2004, 123 (04) :931-938
[9]  
Davies M, 1997, AM J MED GENET, V70, P188, DOI 10.1002/(SICI)1096-8628(19970516)70:2<188::AID-AJMG16>3.0.CO
[10]  
2-F