Literature DB >> 22628065

Facial phenotype at different ages and cardiovascular malformations in children with Williams-Beuren syndrome: a study from India.

Siddaramappa J Patil1, B G Madhusudhan, Sejal Shah, P V Suresh.   

Abstract

Williams-Beuren syndrome (WBS) is one of the microdeletion syndromes associated with distinct facial features, characteristic behavior phenotype (overfriendly behavior), congenital heart disease, and other malformations. Clinical features in WBS are age dependent. It is important to be aware of variable age dependent phenotype, especially facial phenotype due to its crucial role in diagnosis. Here we describe the facial phenotype of WBS at different ages (3 months to 15.1 years) and congenital heart malformations in 27 patients FISH positive for 7q11.23 microdeletion.
Copyright © 2012 Wiley Periodicals, Inc.

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Year:  2012        PMID: 22628065     DOI: 10.1002/ajmg.a.35443

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


  6 in total

1.  Objective differential diagnosis of Noonan and Williams-Beuren syndromes in diverse populations using quantitative facial phenotyping.

Authors:  Antonio R Porras; Marshal Summar; Marius George Linguraru
Journal:  Mol Genet Genomic Med       Date:  2021-03-27       Impact factor: 2.183

2.  Williams-Beuren syndrome in diverse populations.

Authors:  Paul Kruszka; Antonio R Porras; Deise Helena de Souza; Angélica Moresco; Victoria Huckstadt; Ashleigh D Gill; Alec P Boyle; Tommy Hu; Yonit A Addissie; Gary T K Mok; Cedrik Tekendo-Ngongang; Karen Fieggen; Eloise J Prijoles; Pranoot Tanpaiboon; Engela Honey; Ho-Ming Luk; Ivan F M Lo; Meow-Keong Thong; Premala Muthukumarasamy; Kelly L Jones; Khadija Belhassan; Karim Ouldim; Ihssane El Bouchikhi; Laila Bouguenouch; Anju Shukla; Katta M Girisha; Nirmala D Sirisena; Vajira H W Dissanayake; C Sampath Paththinige; Rupesh Mishra; Monisha S Kisling; Carlos R Ferreira; María Beatriz de Herreros; Ni-Chung Lee; Saumya S Jamuar; Angeline Lai; Ee Shien Tan; Jiin Ying Lim; Cham Breana Wen-Min; Neerja Gupta; Stephanie Lotz-Esquivel; Ramsés Badilla-Porras; Dalia Farouk Hussen; Mona O El Ruby; Engy A Ashaat; Siddaramappa J Patil; Leah Dowsett; Alison Eaton; A Micheil Innes; Vorasuk Shotelersuk; Ëben Badoe; Ambroise Wonkam; María Gabriela Obregon; Brian H Y Chung; Milana Trubnykova; Jorge La Serna; Bertha Elena Gallardo Jugo; Miguel Chávez Pastor; Hugo Hernán Abarca Barriga; Andre Megarbane; Beth A Kozel; Mieke M van Haelst; Roger E Stevenson; Marshall Summar; A Adebowale Adeyemo; Colleen A Morris; Danilo Moretti-Ferreira; Marius George Linguraru; Maximilian Muenke
Journal:  Am J Med Genet A       Date:  2018-05       Impact factor: 2.578

3.  Medical genetics and genomic medicine in India: current status and opportunities ahead.

Authors:  Shagun Aggarwal; Shubha R Phadke
Journal:  Mol Genet Genomic Med       Date:  2015-05       Impact factor: 2.183

4.  Prevalence of scoliosis in Williams-Beuren syndrome patients treated at a regional reference center.

Authors:  Marcelo Loquette Damasceno; Alexandre Fogaça Cristante; Raphael Martus Marcon; Tarcísio Eloy Pessoa de Barros Filho
Journal:  Clinics (Sao Paulo)       Date:  2014-07       Impact factor: 2.365

5.  Williams-Beuren syndrome: pitfalls for diagnosis in limited resources setting.

Authors:  Aimé Lumaka; Rita Lukoo; Gerrye Mubungu; Paul Lumbala; Gloire Mbayabo; Aimée Mupuala; Prosper Lukusa Tshilobo; Koenraad Devriendt
Journal:  Clin Case Rep       Date:  2016-02-12

6.  Clinical application of chromosomal microarray analysis for the diagnosis of Williams-Beuren syndrome in Chinese Han patients.

Authors:  Yu Xia; Shufang Huang; Yueheng Wu; Yongchao Yang; Shaoxian Chen; Ping Li; Jian Zhuang
Journal:  Mol Genet Genomic Med       Date:  2018-12-18       Impact factor: 2.183

  6 in total

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