Clinical Follow-Up of Young Adults Affected by Williams Syndrome: Experience of 45 Italian Patients

被引:27
作者
Bedeschi, Maria Francesca [1 ]
Bianchi, Vera [1 ]
Colli, Anna Maria [2 ]
Natacci, Federica [1 ]
Cereda, Anna [3 ]
Milani, Donatella [1 ]
Maitz, Silvia [3 ]
Lalatta, Faustina [1 ]
Selicorni, Angelo [3 ]
机构
[1] Osped Maggiore Policlin, UOD Genet Med, Dipartimento Salute Donna, Fdn IRCCS Ca Granda, I-20122 Milan, Italy
[2] Osped Maggiore Policlin, UO Cardiol, IRCCS Ca Granda, I-20122 Milan, Italy
[3] Univ Milan, Bicocca AOS Gerardo Fdn MBBM, Pediat Clin, Monza, Italy
关键词
ELN gene; management adult patients; rare disease; Williams-Beuren syndrome; BEUREN-SYNDROME; ABNORMALITIES; PREVALENCE;
D O I
10.1002/ajmg.a.33819
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Williams-Beuren syndrome (WBS) is a multisystem disorder that requires ongoing management by a primary care physician familiar with the natural history and specific medical problems associated with the condition. While the natural history of the disease during infancy is well known, data about the adult WBS population have been published only in the last few years, and show a wide range of medical, neurological, and psychiatric problems. We investigated 45 young adult WBS patients (mean age 23 years, range 17-39 years) using a well-coordinated team which included a cardiologist, a nephrologist, an ophthalmologist, an endocrinologist, a gastroenterologist, orthodontist, and orthopedist. Here we describe the clinical features and medical complications in this cohort of patients. Most patients demonstrated a high frequency of multiple organ systems complications, in particular, abnormal body habitus; cardiovascular disease, and hypertension; sensorineural hearing loss; gastrointestinal symptoms including diverticular disease and abnormal glucose tolerance. We offer some suggestions for clinical monitoring which we propose will be useful in the overall care of adults with WBS. (C) 2011 Wiley-Liss, Inc.
引用
收藏
页码:353 / 359
页数:7
相关论文
共 21 条
[11]   Sensorineural hearing loss in children and adults with Williams syndrome [J].
Marler, JA ;
Elfenbein, JL ;
Ryals, BM ;
Urban, Z ;
Netzloff, ML .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2005, 138A (04) :318-327
[12]  
MORRIS CA, 1990, AM J MED GENET, P100
[13]   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
[14]  
Pankau R, 1996, AM J MED GENET, V63, P301, DOI 10.1002/(SICI)1096-8628(19960503)63:1<301::AID-AJMG49>3.0.CO
[15]  
2-P
[16]   Sigmoid diverticulitis in patients with Williams-Beuren syndrome: Relatively high prevalence and high complication rate in young adults with the syndrome [J].
Partsch, CJ ;
Siebert, R ;
Caliebe, A ;
Gosch, A ;
Wessel, A ;
Pankau, R .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2005, 137A (01) :52-54
[17]   Diagnosis and management of medical problems in adults with Williams-Beuren syndrome [J].
Pober, Barbara R. ;
Morris, Colleen A. .
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS, 2007, 145C (03) :280-290
[18]   Thyroid anomalies in Williams syndrome: Investigation of 95 patients [J].
Selicorni, A ;
Fratoni, A ;
Pavesi, MA ;
Bottigelli, M ;
Arnaboldi, E ;
Milani, D .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2006, 140A (10) :1098-1101
[19]  
Sforzini Cinzia, 2002, Pediatric Nephrology, V17, P899
[20]   Prevalence estimation of Williams syndrome [J].
Stromme, P ;
Bjornstad, PG ;
Ramstad, K .
JOURNAL OF CHILD NEUROLOGY, 2002, 17 (04) :269-271