Literature DB >> 15534874

Multisystem study of 20 older adults with Williams syndrome.

Elizabeth M Cherniske1, Thomas O Carpenter, Cheryl Klaiman, Eytan Young, Joel Bregman, Karl Insogna, Robert T Schultz, Barbara R Pober.   

Abstract

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.

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Mesh:

Year:  2004        PMID: 15534874     DOI: 10.1002/ajmg.a.30400

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  67 in total

1.  High prevalence of diabetes and pre-diabetes in adults with Williams syndrome.

Authors:  B R Pober; E Wang; S Caprio; K F Petersen; C Brandt; T Stanley; L R Osborne; J Dzuria; B Gulanski
Journal:  Am J Med Genet C Semin Med Genet       Date:  2010-05-15       Impact factor: 3.908

2.  Transcriptome profile in Williams-Beuren syndrome lymphoblast cells reveals gene pathways implicated in glucose intolerance and visuospatial construction deficits.

Authors:  Anna Antonell; Mireia Vilardell; Luis A Pérez Jurado
Journal:  Hum Genet       Date:  2010-04-17       Impact factor: 4.132

3.  Genetic contributions to white matter architecture revealed by diffusion tensor imaging in Williams syndrome.

Authors:  Stefano Marenco; Michael A Siuta; J Shane Kippenhan; Samuel Grodofsky; Wei-Li Chang; Philip Kohn; Carolyn B Mervis; Colleen A Morris; Daniel R Weinberger; Andreas Meyer-Lindenberg; Carlo Pierpaoli; Karen Faith Berman
Journal:  Proc Natl Acad Sci U S A       Date:  2007-09-07       Impact factor: 11.205

4.  Children with 7q11.23 duplication syndrome: psychological characteristics.

Authors:  Carolyn B Mervis; Bonita P Klein-Tasman; Myra J Huffman; Shelley L Velleman; C Holley Pitts; Danielle R Henderson; Janet Woodruff-Borden; Colleen A Morris; Lucy R Osborne
Journal:  Am J Med Genet A       Date:  2015-04-21       Impact factor: 2.802

5.  Frizzled-4 is required for normal bone acquisition despite compensation by Frizzled-8.

Authors:  Priyanka Kushwaha; Soohyun Kim; Gabrielle E Foxa; Megan N Michalski; Bart O Williams; Ryan E Tomlinson; Ryan C Riddle
Journal:  J Cell Physiol       Date:  2020-01-27       Impact factor: 6.384

Review 6.  Heterogeneous phenotype in children affected by non-autoimmune hypothyroidism: an update.

Authors:  M C Vigone; M Di Frenna; G Weber
Journal:  J Endocrinol Invest       Date:  2015-04-28       Impact factor: 4.256

7.  Abnormalities in neural processing of emotional stimuli in Williams syndrome vary according to social vs. non-social content.

Authors:  Karen E Muñoz; Andreas Meyer-Lindenberg; Ahmad R Hariri; Carolyn B Mervis; Venkata S Mattay; Colleen A Morris; Karen Faith Berman
Journal:  Neuroimage       Date:  2009-12-11       Impact factor: 6.556

8.  Hypercalcemia in Patients with Williams-Beuren Syndrome.

Authors:  Sampat Sindhar; Michael Lugo; Mark D Levin; Joshua R Danback; Benjamin D Brink; Eric Yu; Dennis J Dietzen; Amy L Clark; Carolyn A Purgert; Jessica L Waxler; Robert W Elder; Barbara R Pober; Beth A Kozel
Journal:  J Pediatr       Date:  2016-08-26       Impact factor: 4.406

Review 9.  Mechanisms and treatment of cardiovascular disease in Williams-Beuren syndrome.

Authors:  Barbara R Pober; Mark Johnson; Zsolt Urban
Journal:  J Clin Invest       Date:  2008-05       Impact factor: 14.808

10.  Hemizygosity at the NCF1 gene in patients with Williams-Beuren syndrome decreases their risk of hypertension.

Authors:  Miguel Del Campo; Anna Antonell; Luis F Magano; Francisco J Muñoz; Raquel Flores; Mònica Bayés; Luis A Pérez Jurado
Journal:  Am J Hum Genet       Date:  2006-01-31       Impact factor: 11.025

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