Literature DB >> 31964759

Health Care Supervision for Children With Williams Syndrome.

Colleen A Morris1, Stephen R Braddock2.   

Abstract

This set of recommendations is designed to assist the pediatrician in caring for children with Williams syndrome (WS) who were diagnosed by using clinical features and with chromosome 7 microdeletion confirmed by fluorescence in situ hybridization, chromosome microarray, or multiplex ligation-dependent probe amplification. The recommendations in this report reflect review of the current literature, including previously peer-reviewed and published management suggestions for WS, as well as the consensus of physicians and psychologists with expertise in the care of individuals with WS. These general recommendations for the syndrome do not replace individualized medical assessment and treatment.
Copyright © 2020 by the American Academy of Pediatrics.

Entities:  

Keywords:  ADHD; SVAS; WS; Williams syndrome; attention-deficit/hyperactivity disorder; supravalvular aortic stenosis

Year:  2020        PMID: 31964759     DOI: 10.1542/peds.2019-3761

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  11 in total

1.  [Early motor development in children with Williams syndrome].

Authors:  Ji-Yang Shen; Fang-Fang Li; Chai Ji; Wei-Jun Chen; Dan Yao
Journal:  Zhongguo Dang Dai Er Ke Za Zhi       Date:  2022 Sept 15

2.  Innate frequency-discrimination hyperacuity in Williams-Beuren syndrome mice.

Authors:  Christopher M Davenport; Brett J W Teubner; Seung Baek Han; Mary H Patton; Tae-Yeon Eom; Dusan Garic; Benjamin J Lansdell; Abbas Shirinifard; Ti-Cheng Chang; Jonathon Klein; Shondra M Pruett-Miller; Jay A Blundon; Stanislav S Zakharenko
Journal:  Cell       Date:  2022-09-23       Impact factor: 66.850

Review 3.  Renovascular hypertension in pediatric patients: update on diagnosis and management.

Authors:  Juliana Lacerda de Oliveira Campos; Letícia Bitencourt; Ana Luisa Pedrosa; Diego Ferreira Silva; Filipe Ji Jen Lin; Lucas Teixeira de Oliveira Dias; Ana Cristina Simões E Silva
Journal:  Pediatr Nephrol       Date:  2021-04-13       Impact factor: 3.714

4.  Shared developmental gait disruptions across two mouse models of neurodevelopmental disorders.

Authors:  Joseph D Dougherty; Susan E Maloney; Rachel M Rahn; Claire T Weichselbaum; David H Gutmann
Journal:  J Neurodev Disord       Date:  2021-03-20       Impact factor: 4.074

Review 5.  Hashimoto's Thyroiditis and Graves' Disease in Genetic Syndromes in Pediatric Age.

Authors:  Celeste Casto; Giorgia Pepe; Alessandra Li Pomi; Domenico Corica; Tommaso Aversa; Malgorzata Wasniewska
Journal:  Genes (Basel)       Date:  2021-02-04       Impact factor: 4.096

6.  Revealing Chronic Granulomatous Disease in a Patient With Williams-Beuren Syndrome Using Whole Exome Sequencing.

Authors:  Adiratna Mat Ripen; Mei Yee Chiow; Prakash Rao Rama Rao; Saharuddin Bin Mohamad
Journal:  Front Immunol       Date:  2021-11-04       Impact factor: 7.561

7.  Neural Networks for Classification and Image Generation of Aging in Genetic Syndromes.

Authors:  Dat Duong; Ping Hu; Cedrik Tekendo-Ngongang; Suzanna E Ledgister Hanchard; Simon Liu; Benjamin D Solomon; Rebekah L Waikel
Journal:  Front Genet       Date:  2022-04-11       Impact factor: 4.772

8.  A case report of interventricular hemorrhage in William-Beuren syndrome.

Authors:  Abdullah Alghobaishi; Ahmed Hafez Mousa; Haleema Sami Almonaye; Tasneem Khalid Maghrebi; Abeer Amin; Fawziah Alzaid Al Sharif
Journal:  Ann Med Surg (Lond)       Date:  2022-08-05

Review 9.  Williams syndrome.

Authors:  Beth A Kozel; Boaz Barak; Chong Ae Kim; Carolyn B Mervis; Lucy R Osborne; Melanie Porter; Barbara R Pober
Journal:  Nat Rev Dis Primers       Date:  2021-06-17       Impact factor: 65.038

Review 10.  Autoimmune Thyroid Disease in Specific Genetic Syndromes in Childhood and Adolescence.

Authors:  Eleni Magdalini Kyritsi; Christina Kanaka-Gantenbein
Journal:  Front Endocrinol (Lausanne)       Date:  2020-08-19       Impact factor: 5.555

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