Literature DB >> 6809950

A slowly progressive degenerative condition characterized by mental deficiency, wasting of limb musculature and bone abnormalities, including ossification of the pinnae.

D A Primrose.   

Abstract

A condition is described in a 33-year-old Caucasian male in which there is severe mental deficiency present from an early age. There is non-progressive hydrocephaly and the eye findings include posterior polar cataracts. There is slowly progressive muscle wasting of the limbs along with degenerative bone changes. Ossification has occurred in the pinnae. Secondary sexual characteristics are underdeveloped and there is a low normal serum testosterone. The parents are not related and there is no similar occurrence in the family. Biochemical investigations do not show any abnormality, and the chromosome picture is that of a normal male karyotype. The case appears to be unique.

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Mesh:

Year:  1982        PMID: 6809950     DOI: 10.1111/j.1365-2788.1982.tb00133.x

Source DB:  PubMed          Journal:  J Ment Defic Res        ISSN: 0022-264X


  8 in total

1.  Motor tics, stereotypies, and self-flagellation in primrose syndrome.

Authors:  P Dalal; N D Leslie; N M Lindor; D L Gilbert; A J Espay
Journal:  Neurology       Date:  2010-07-20       Impact factor: 9.910

2.  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

Review 3.  Ossification of the external ear: a case report and review of the literature.

Authors:  Johannes J Manni; Lysandra C M Berénos-Riley
Journal:  Eur Arch Otorhinolaryngol       Date:  2005-06-18       Impact factor: 2.503

4.  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

5.  Zbtb20 Restrains CD8 T Cell Immunometabolism and Restricts Memory Differentiation and Antitumor Immunity.

Authors:  Yanbo Sun; Nicholas K Preiss; Kristine B Valenteros; Yasmin Kamal; Young-Kwang Usherwood; H Robert Frost; Edward J Usherwood
Journal:  J Immunol       Date:  2020-09-30       Impact factor: 5.422

6.  Posterior polar cataract: A review.

Authors:  Hatem Kalantan
Journal:  Saudi J Ophthalmol       Date:  2011-05-07

7.  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

8.  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

  8 in total

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