Literature DB >> 16913274

Rubinstein-Taybi syndrome: an immune deficiency as a cause for recurrent infections.

David R Naimi1, Jose Munoz, Jack Rubinstein, Robert W Hostoffer.   

Abstract

Rubinstein-Tabyi Syndrome (RTS) is characterized by broad toes, broad thumbs, facial dysmorphisms, and mental retardation. The syndrome has been shown in some patients to be associated with break points in and microdeletions of chromosome 16p13.3. It is estimated that approximately 75% of patients with RTS experience recurrent respiratory infections. In this study, three patients thought to have RTS and recurrent infections were evaluated for an immunologic deficiency. All three patients showed a polysaccharide antibody response deficit. We conclude that a primary immune deficiency may exist in the remainder of the RTS population and may explain the reason for the propensity for recurrent infections. Aggressive investigation and management in patients with RTS may further determine the mechanism of this deficiency and enhance the quality of life of these patients.

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Year:  2006        PMID: 16913274     DOI: 10.2500/aap.2006.27.2864

Source DB:  PubMed          Journal:  Allergy Asthma Proc        ISSN: 1088-5412            Impact factor:   2.587


  5 in total

1.  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

2.  Rubinstein-Taybi Syndrome in a Filipino Infant with a Novel CREBBP Gene Pathogenic Variant.

Authors:  Rhea Camille R Yumul; Mary Anne D Chiong
Journal:  Case Rep Genet       Date:  2022-05-21

Review 3.  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 4.  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

5.  Rubinstein-Taybi syndrome in a Saudi boy with distinct features and variants in both the CREBBP and EP300 genes: a case report.

Authors:  Mohammad M Al-Qattan; Abdulaziz Jarman; Atif Rafique; Zuhair N Al-Hassnan; Heba M Al-Qattan
Journal:  BMC Med Genet       Date:  2019-01-11       Impact factor: 2.103

  5 in total

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