Literature DB >> 21671385

Adults with Rubinstein-Taybi syndrome.

Cathy A Stevens1, Jill Pouncey, Darcy Knowles.   

Abstract

Information in the medical literature regarding adults with genetic syndromes is limited, making the care of these patients challenging. We conducted a questionnaire study of adults with Rubinstein-Taybi syndrome that addressed medical problems, education, independence, and behavior. The most common medical problems included short stature, obesity, visual difficulties, keloids, eating problems, spine curvature, and joint problems. The adults had typically moderate mental retardation, but most achieved some independence in self-care and communication; many participated in supported work situations. However, approximately one-third were said to have some decreased abilities over time. Behavior problems were common and often worsened with age. Very few of the study participants were seeing a geneticist as an adult. Long-term involvement of geneticists and education of adult primary care providers may help with many of the challenges facing adults with RTS and their families.
Copyright © 2011 Wiley-Liss, Inc.

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Year:  2011        PMID: 21671385     DOI: 10.1002/ajmg.a.34058

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


  16 in total

1.  Rubinstein-Taybi syndrome with scoliosis treated with single-stage posterior spinal fusion: illustrative case.

Authors:  Takeshi Imai; Daisuke Sakai; Jordy Schol; Toshihiro Nagai; Akihiko Hiyama; Hiroyuki Katoh; Masato Sato; Masahiko Watanabe
Journal:  J Neurosurg Case Lessons       Date:  2021-03-15

2.  The natural history of adults with Rubinstein-Taybi syndrome: a families-reported experience.

Authors:  Sofia Douzgou; Janet Dell'Oro; Cristina Rodriguez Fonseca; Alessandra Rei; Jo Mullins; Isabelle Jusiewicz; Sylvia Huisman; Brittany N Simpson; Klea Vyshka; Donatella Milani; Oliver Bartsch; Didier Lacombe; Sixto García-Miñaúr; Raoul C M Hennekam
Journal:  Eur J Hum Genet       Date:  2022-04-06       Impact factor: 5.351

3.  A Behavioural Assessment of Social Anxiety and Social Motivation in Fragile X, Cornelia de Lange and Rubinstein-Taybi Syndromes.

Authors:  Hayley Crawford; Joanna Moss; Laura Groves; Robyn Dowlen; Lisa Nelson; Donna Reid; Chris Oliver
Journal:  J Autism Dev Disord       Date:  2020-01

4.  The association of neural axis and craniovertebral junction anomalies with scoliosis in Rubinstein-Taybi syndrome.

Authors:  Carlo Giussani; Angelo Selicorni; Chiara Fossati; Pablo Ingelmo; Francesco Canonico; Andrea Landi; Andrea Trezza; Matteo Riva; Erik P Sganzerla
Journal:  Childs Nerv Syst       Date:  2012-08-23       Impact factor: 1.475

Review 5.  Ultra-Rare Syndromes: The Example of Rubinstein-Taybi Syndrome.

Authors:  Silvia Spena; Cristina Gervasini; Donatella Milani
Journal:  J Pediatr Genet       Date:  2015-09-28

Review 6.  Malformation syndromes associated with disorders of sex development.

Authors:  John M Hutson; Sonia R Grover; Michele O'Connell; Samuel D Pennell
Journal:  Nat Rev Endocrinol       Date:  2014-06-10       Impact factor: 43.330

7.  Keloid scarring: understanding the genetic basis, advances, and prospects.

Authors:  Ahmad Sukari Halim; Azadeh Emami; Iman Salahshourifar; Thirumulu Ponnuraj Kannan
Journal:  Arch Plast Surg       Date:  2012-05-10

Review 8.  Rubinstein-Taybi syndrome: clinical features, genetic basis, diagnosis, and management.

Authors:  Donatella Milani; Francesca Maria Paola Manzoni; Lidia Pezzani; Paola Ajmone; Cristina Gervasini; Francesca Menni; Susanna Esposito
Journal:  Ital J Pediatr       Date:  2015-01-20       Impact factor: 2.638

9.  Diverse Profiles of Anxiety Related Disorders in Fragile X, Cornelia de Lange and Rubinstein-Taybi Syndromes.

Authors:  Hayley Crawford; Jane Waite; Chris Oliver
Journal:  J Autism Dev Disord       Date:  2017-12

10.  Benign and malignant tumors in Rubinstein-Taybi syndrome.

Authors:  Max V Boot; Martine J van Belzen; Lucy I Overbeek; Nathalie Hijmering; Matias Mendeville; Quinten Waisfisz; Pieter Wesseling; Raoul C Hennekam; Daphne de Jong
Journal:  Am J Med Genet A       Date:  2018-01-23       Impact factor: 2.802

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