Literature DB >> 2118774

Broad thumb-hallux (Rubinstein-Taybi) syndrome 1957-1988.

J H Rubinstein1.   

Abstract

This presentation records the early history of the description of the broad thumb-hallux syndrome and attempts to update the current state of knowledge about this syndrome. Information was collected and reviewed on 571 individuals from the world literature, from communications with colleagues and families of affected individuals, and from personal observation. The diagnosis was established in most cases by confirming the concurrence of the constellation of major diagnostic criteria, including broad short terminal phalanges of the thumbs and halluces, with or without angulation deformity; characteristic facial appearance with beaked or straight nose, antimongoloid slant of palpebral fissures, apparent or clinical hypertelorism and grimacing smile; stature and head circumference (OFC) below 50th centile; mental, motor, social, and language retardation; stiff awkward gait; and incomplete or delayed descent of testes in males. Information on associated clinical factors, familial occurrence, and cytogenetic findings is presented.

Entities:  

Mesh:

Year:  1990        PMID: 2118774     DOI: 10.1002/ajmg.1320370603

Source DB:  PubMed          Journal:  Am J Med Genet Suppl        ISSN: 1040-3787


  22 in total

Review 1.  The sonic hedgehog-patched-gli pathway in human development and disease.

Authors:  E H Villavicencio; D O Walterhouse; P M Iannaccone
Journal:  Am J Hum Genet       Date:  2000-09-21       Impact factor: 11.025

2.  Genetic heterogeneity in Rubinstein-Taybi syndrome: delineation of the phenotype of the first patients carrying mutations in EP300.

Authors:  Deborah Bartholdi; Jeroen H Roelfsema; Francesco Papadia; Martijn H Breuning; Dunja Niedrist; Raoul C Hennekam; Albert Schinzel; Dorien J M Peters
Journal:  J Med Genet       Date:  2007-01-12       Impact factor: 6.318

3.  Rubinstein-Taybi syndrome with humoral and cellular defects: a case report.

Authors:  A Villella; D Bialostocky; E Lori; H Meyerson; R W Hostoffer
Journal:  Arch Dis Child       Date:  2000-10       Impact factor: 3.791

4.  Rubinstein-Taybi Syndrome Associated with Pituitary Macroadenoma: A Case Report.

Authors:  Yasamin Olyaei; J Manuel Sarmiento; Serguei I Bannykh; Doniel Drazin; Robert T Naruse; Wesley King
Journal:  Cureus       Date:  2017-04-11

5.  Calcium/calmodulin-dependent protein kinase IV mediates distinct features of basal and activity-dependent dendrite complexity.

Authors:  T Nagendran; L R Hardy
Journal:  Neuroscience       Date:  2011-10-01       Impact factor: 3.590

6.  Downregulation of p300 gene expression in airway mesenchyme of nitrofen-induced hypoplastic lungs.

Authors:  Hiromizu Takahashi; Florian Friedmacher; Naho Fujiwara; Alejandro Hofmann; Toshiaki Takahashi; Prem Puri
Journal:  Pediatr Surg Int       Date:  2014-04       Impact factor: 1.827

7.  Rubinstein-taybi syndrome: a female patient with a de novo reciprocal translocation t(2; 16)(q36.3; p13.3) and dysgranulopoiesis.

Authors:  Leuridan Cavalcante Torres; Maria de Lourdes Lopes Chauffaille; Thomaz Pileggi Delboni; Thelma Suely Okay; Magda Carneiro-Sampaio; Sofia Sugayama
Journal:  Clinics (Sao Paulo)       Date:  2010       Impact factor: 2.365

8.  New dysmorphic features in Rubinstein-Taybi syndrome.

Authors:  D Kanjilal; M A Basir; R S Verma; B K Rajegowda; R Lala; A Nagaraj
Journal:  J Med Genet       Date:  1992-09       Impact factor: 6.318

Review 9.  Ultra-Rare Syndromes: The Example of Rubinstein-Taybi Syndrome.

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

10.  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

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