Literature DB >> 34909074

Rubinstein-Taybi syndrome: a rare case report of a female child emphasizing physiotherapy on gross motor function.

Rakesh Krishna Kovela1, Mohammad Irshad Qureshi2, Ansar Manakandathil3, Mukesh Kumar Sinha4, Neethu Dinesh4, Pallavi Harjpal1.   

Abstract

Rubinstein-Taybi syndrome (RSTS) is a chromosomal segment 16p13.3 microdeletion syndrome and is characterized by CREBBP gene mutations, delay in the development of height and weight, distinctive facial features, broad and sometimes angulated thumbs and halluces, short stature, and intellectual impairment that is mild to extreme. Current literature emphasizes mainly medical, dental, and psychiatric issues in RSTS and there is no retrievable literature on physiotherapy and its role in improving motor function in RSTS. The present case report is of a baby girl of 17 months suspected case of RSTS, presented with all the features of RSTS. Delay in the acquisition of skills and development were the chief complaints. We designed a 12-week treatment regimen that concentrated mainly on transitions using principles of neurodevelopmental therapy. Gross motor function measure (GMFM 88) was taken pre- and post-treatment which showed tremendous improvement. This is the first study on the role of physiotherapy in RSTS. Copyright: Rakesh Krishna Kovela et al.

Entities:  

Keywords:  Rubinstein-Taybi syndrome; case report; delayed development; physical activities; physiotherapy

Mesh:

Substances:

Year:  2021        PMID: 34909074      PMCID: PMC8607943          DOI: 10.11604/pamj.2021.40.85.31240

Source DB:  PubMed          Journal:  Pan Afr Med J


  8 in total

1.  Submicroscopic deletions at 16p13.3 in Rubinstein-Taybi syndrome: frequency and clinical manifestations in a North American population.

Authors:  R Wallerstein; C E Anderson; B Hay; P Gupta; L Gibas; K Ansari; F S Cowchock; V Weinblatt; C Reid; A Levitas; L Jackson
Journal:  J Med Genet       Date:  1997-03       Impact factor: 6.318

2.  Rubinstein-Taybi syndrome with epidermal nevus: a case report.

Authors:  C Schepis; D Greco; M Siragusa; D Batolo; C Romano
Journal:  Pediatr Dermatol       Date:  2001 Jan-Feb       Impact factor: 1.588

3.  Talon cusps: a dental anomaly in the Rubinstein-Taybi syndrome.

Authors:  D G Gardner; S S Girgis
Journal:  Oral Surg Oral Med Oral Pathol       Date:  1979-06

4.  Rubinstein-Taybi syndrome with de novo reciprocal translocation t(2;16)(p13.3;p13.3).

Authors:  K Imaizumi; Y Kuroki
Journal:  Am J Med Genet       Date:  1991-03-15

5.  Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP.

Authors:  F Petrij; R H Giles; H G Dauwerse; J J Saris; R C Hennekam; M Masuno; N Tommerup; G J van Ommen; R H Goodman; D J Peters
Journal:  Nature       Date:  1995-07-27       Impact factor: 49.962

6.  Effect of intensive neurodevelopmental treatment in gross motor function of children with cerebral palsy.

Authors:  Nikos Tsorlakis; Christina Evaggelinou; George Grouios; Charalambos Tsorbatzoudis
Journal:  Dev Med Child Neurol       Date:  2004-11       Impact factor: 5.449

Review 7.  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

  8 in total

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