Literature DB >> 2920750

Rubinstein-Taybi syndrome in a mother and son.

R C Hennekam1, E J Lommen, J L Strengers, H G Van Spijker, T M Jansen-Kokx.   

Abstract

The Rubinstein-Taybi syndrome is a condition characterized by mental retardation, typical facial changes and broad thumbs and big toes. The cause is unknown; almost all cases are sporadic. We describe a mother and son with Rubinstein-Taybi syndrome. Literature search documented at least 413 cases with 558 sibs. An affected offspring has occurred at least twice, possibly six times. In 45 yet undescribed Dutch cases no recurrence was found in 94 sibs. A submicroscopic chromosome deletion seems the most probable explanation, but other alternatives may be possible.

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Year:  1989        PMID: 2920750     DOI: 10.1007/BF00595907

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  30 in total

1.  [Arched, clubbed thumb in strong abduction-extension & other concomitant symptoms].

Authors:  J MICHAIL; J MATSOUKAS; S THEODOROU
Journal:  Rev Chir Orthop Reparatrice Appar Mot       Date:  1957 Apr-Jun

2.  [Rubinstein-Taybi-Syndrome in premature, probably identical twins].

Authors:  W Holthusen; C Panteliadis
Journal:  Monatsschr Kinderheilkd       Date:  1971-09

3.  The Rubinstein-Taybi syndrome.

Authors:  C J Padfield; M W Partington; N E Simpson
Journal:  Arch Dis Child       Date:  1968-02       Impact factor: 3.791

4.  [Rubinstein-Taybi syndrome. Discussion of incomplete and familial forms].

Authors:  F Hayem; J Boisse; M O Rethore; M Labrune; M Hambourg; P Mozziconacci
Journal:  Pediatrie       Date:  1970 Jan-Feb

Review 5.  Rubinstein-Taybi syndrome.

Authors:  A C Berry
Journal:  J Med Genet       Date:  1987-09       Impact factor: 6.318

6.  The Rubinstein-Taybi syndrome: occurrence in two sets of identical twins.

Authors:  M Baraitser; M A Preece
Journal:  Clin Genet       Date:  1983-04       Impact factor: 4.438

7.  [The Rubinstein-Taybi syndrome. Presentation of 2 new cases].

Authors:  T De Toni; G Cavaliere; M Cortese; R Gastaldi; L Carozzino; M T Duillo
Journal:  Minerva Pediatr       Date:  1982-09-30       Impact factor: 1.312

8.  Monozygotic twinning and structural defects.

Authors:  A A Schinzel; D W Smith; J R Miller
Journal:  J Pediatr       Date:  1979-12       Impact factor: 4.406

9.  [The Rubenstein-Taybi syndrome. Apropos of a case].

Authors:  G Jéliu; G Saint-Rome
Journal:  Union Med Can       Date:  1967-01

10.  Monozygotic twins discordant for rubinstein-taybi syndrome.

Authors:  T Kajii; K Hagiwara; M Tsukahara; H Nakajima; Y Fukuda
Journal:  J Med Genet       Date:  1981-08       Impact factor: 6.318

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  9 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: A Rare Case Report.

Authors:  Suyash S Tomar; Bhagyashree B Supekar; Jayesh Mukhi; Rajesh Pratap Singh
Journal:  Indian Dermatol Online J       Date:  2020-03-09

3.  Diagnostic analysis of the Rubinstein-Taybi syndrome: five cosmids should be used for microdeletion detection and low number of protein truncating mutations.

Authors:  F Petrij; H G Dauwerse; R I Blough; R H Giles; J J van der Smagt; R Wallerstein; P D Maaswinkel-Mooy; C D van Karnebeek; G J van Ommen; A van Haeringen; J H Rubinstein; H M Saal; R C Hennekam; D J Peters; M H Breuning
Journal:  J Med Genet       Date:  2000-03       Impact factor: 6.318

4.  Deletion at chromosome 16p13.3 as a cause of Rubinstein-Taybi syndrome: clinical aspects.

Authors:  R C Hennekam; M Tilanus; B C Hamel; H Voshart-van Heeren; E C Mariman; S E van Beersum; M J van den Boogaard; M H Breuning
Journal:  Am J Hum Genet       Date:  1993-02       Impact factor: 11.025

5.  Novel cAMP binding protein-BP (CREBBP) mutation in a girl with Rubinstein-Taybi syndrome, GH deficiency, Arnold Chiari malformation and pituitary hypoplasia.

Authors:  Pierluigi Marzuillo; Anna Grandone; Ruggero Coppola; Domenico Cozzolino; Adalgisa Festa; Federica Messa; Caterina Luongo; Emanuele Miraglia Del Giudice; Laura Perrone
Journal:  BMC Med Genet       Date:  2013-02-23       Impact factor: 2.103

Review 6.  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

7.  A novel CREBBP mutation and its phenotype in a case of Rubinstein-Taybi syndrome.

Authors:  Qian Wang; Cong Wang; Wen Bin Wei; Wei Ning Rong; Xiang Yu Shi
Journal:  BMC Med Genomics       Date:  2022-08-19       Impact factor: 3.622

8.  First case report of inherited Rubinstein-Taybi syndrome associated with a novel EP300 variant.

Authors:  María López; Verónica Seidel; Paula Santibáñez; Cristina Cervera-Acedo; Pedro Castro-de Castro; Elena Domínguez-Garrido
Journal:  BMC Med Genet       Date:  2016-12-13       Impact factor: 2.103

Review 9.  Rubinstein-Taybi Syndrome: A Model of Epigenetic Disorder.

Authors:  Julien Van Gils; Frederique Magdinier; Patricia Fergelot; Didier Lacombe
Journal:  Genes (Basel)       Date:  2021-06-24       Impact factor: 4.096

  9 in total

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