Literature DB >> 8992092

[Kohlschütter syndrome--an example of a rare progressive neuroectodermal disease. Case report and review of the literature].

T Wygold1, G Kurlemann, G Schuierer.   

Abstract

Kohlschütter's syndrome is a combination of amelogenesis imperfecta, progressive mental retardation and epileptic seizures. We report on a patient with typical signs of this syndrome. Beneath severe enamal defects of teeth, the patient has been suffering from progressive mental and motoric retardation from the age of six months. Although there is pathologic activity in EEG, seizures have not yet appeared. MRT shows distinct signs of cerebral atrophy. Apart from this patient 15 patients in 4 families have been reported up to now in literature. The article compares diagnostic results in this case with those reported in literature.

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Year:  1996        PMID: 8992092     DOI: 10.1055/s-2008-1046481

Source DB:  PubMed          Journal:  Klin Padiatr        ISSN: 0300-8630            Impact factor:   1.349


  4 in total

1.  Mutations in ROGDI Cause Kohlschütter-Tönz Syndrome.

Authors:  Anna Schossig; Nicole I Wolf; Christine Fischer; Maria Fischer; Gernot Stocker; Stephan Pabinger; Andreas Dander; Bernhard Steiner; Otmar Tönz; Dieter Kotzot; Edda Haberlandt; Albert Amberger; Barbara Burwinkel; Katharina Wimmer; Christine Fauth; Caspar Grond-Ginsbach; Martin J Koch; Annette Deichmann; Christof von Kalle; Claus R Bartram; Alfried Kohlschütter; Zlatko Trajanoski; Johannes Zschocke
Journal:  Am J Hum Genet       Date:  2012-03-15       Impact factor: 11.025

2.  A nonsense mutation in the human homolog of Drosophila rogdi causes Kohlschutter-Tonz syndrome.

Authors:  Adi Mory; Efrat Dagan; Barbara Illi; Philippe Duquesnoy; Shikma Mordechai; Ishai Shahor; Sveva Romani; Nivin Hawash-Moustafa; Hanna Mandel; Enza M Valente; Serge Amselem; Ruth Gershoni-Baruch
Journal:  Am J Hum Genet       Date:  2012-04-06       Impact factor: 11.025

3.  Kohlschütter-Tönz Syndrome - Report of an additional case.

Authors:  Wilfredo A González-Arriagada; Román Carlos-Bregni; Elisa Contreras; Oslei P Almeida; Marcio A Lopes
Journal:  J Clin Exp Dent       Date:  2013-04-01

4.  Kohlschütter-Tönz syndrome: mutations in ROGDI and evidence of genetic heterogeneity.

Authors:  Arianna Tucci; Eleanna Kara; Anna Schossig; Nicole I Wolf; Vincent Plagnol; Katherine Fawcett; Coro Paisán-Ruiz; Matthew Moore; Dena Hernandez; Sebastiano Musumeci; Michael Tennison; Raoul Hennekam; Silvia Palmeri; Alessandro Malandrini; Salmo Raskin; Dian Donnai; Corina Hennig; Andreas Tzschach; Roel Hordijk; Thomas Bast; Katharina Wimmer; Chien-Ning Lo; Simon Shorvon; Heather Mefford; Evan E Eichler; Roger Hall; Ian Hayes; John Hardy; Andrew Singleton; Johannes Zschocke; Henry Houlden
Journal:  Hum Mutat       Date:  2012-11-27       Impact factor: 4.878

  4 in total

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