Literature DB >> 21567911

Additional features of unique Primrose syndrome phenotype.

Daniel Rocha Carvalho1, Carlos Eduardo Speck-Martins.   

Abstract

Primrose syndrome is a unique condition of intellectual disability, dysmorphic facial features, and specific minor abnormalities including large calcified ear auricles. Only six patients have been previously reported. We describe a Brazilian boy with the striking similar facies and the main clinical findings that reinforced the singular phenotype of this rare disorder. The key features of all patients already published were compared. Our young patient has abnormalities that were not observed in preceding reports: nail dysplasia and hyperuricemia.
Copyright © 2011 Wiley-Liss, Inc.

Entities:  

Mesh:

Year:  2011        PMID: 21567911     DOI: 10.1002/ajmg.a.33955

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


  5 in total

1.  De novo nonsense and frameshift variants of TCF20 in individuals with intellectual disability and postnatal overgrowth.

Authors:  Johanna Schäfgen; Kirsten Cremer; Jessica Becker; Thomas Wieland; Alexander M Zink; Sarah Kim; Isabelle C Windheuser; Martina Kreiß; Stefan Aretz; Tim M Strom; Dagmar Wieczorek; Hartmut Engels
Journal:  Eur J Hum Genet       Date:  2016-07-20       Impact factor: 4.246

2.  Mutations in ZBTB20 cause Primrose syndrome.

Authors:  Viviana Cordeddu; Bert Redeker; Emilia Stellacci; Aldo Jongejan; Alessandra Fragale; Ted E J Bradley; Massimiliano Anselmi; Andrea Ciolfi; Serena Cecchetti; Valentina Muto; Laura Bernardini; Meron Azage; Daniel R Carvalho; Alberto J Espay; Alison Male; Anna-Maja Molin; Renata Posmyk; Carla Battisti; Alberto Casertano; Daniela Melis; Antoine van Kampen; Frank Baas; Marcel M Mannens; Gianfranco Bocchinfuso; Lorenzo Stella; Marco Tartaglia; Raoul C Hennekam
Journal:  Nat Genet       Date:  2014-07-13       Impact factor: 38.330

Review 3.  Auricular ossification: A newly recognized feature of osteoprotegerin-deficiency juvenile Paget disease.

Authors:  Gary S Gottesman; Katherine L Madson; William H McAlister; Angela Nenninger; Deborah Wenkert; Steven Mumm; Michael P Whyte
Journal:  Am J Med Genet A       Date:  2016-01-14       Impact factor: 2.802

4.  Unique skeletal manifestations in patients with Primrose syndrome.

Authors:  Veronica Arora; Eyby Leon; Jullianne Diaz; Hanne Buciek Hove; Daniel Rocha Carvalho; Kenji Kurosawa; Naoto Nishimura; Gen Nishimura; Renu Saxena; Carlos Ferreira; Ratna Dua Puri; Ishwar C Verma
Journal:  Eur J Med Genet       Date:  2020-05-27       Impact factor: 2.465

5.  Primrose syndrome: Characterization of the phenotype in 42 patients.

Authors:  Daniela Melis; Daniel Carvalho; Tina Barbaro-Dieber; Alberto J Espay; Michael J Gambello; Blanca Gener; Erica Gerkes; Marrit M Hitzert; Hanne B Hove; Sandra Jansen; Petr E Jira; Katherine Lachlan; Leonie A Menke; Vinodh Narayanan; Damara Ortiz; Eline Overwater; Renata Posmyk; Keri Ramsey; Alessandro Rossi; Renata Lazari Sandoval; Constance Stumpel; Kyra E Stuurman; Viviana Cordeddu; Peter Turnpenny; Pietro Strisciuglio; Marco Tartaglia; Sheela Unger; Todd Waters; Clare Turnbull; Raoul C Hennekam
Journal:  Clin Genet       Date:  2020-04-20       Impact factor: 4.438

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.