Literature DB >> 20013277

[Tapetoretinal dystrophy and unusual facial features in an 8-year-old boy].

S Kramer1, B Seitz, B Käsmann-Kellner.   

Abstract

An 8-year-old boy showed multiple cardiovascular and urinogenital anomalies, neurological problems as well as endocrinological abnormalities even shortly after birth. The patient had ophthalmological peculiarities, such as eyelid cleft configuration, tapetoretinal dystrophy, retinal visual atrophy, early childhood converging strabismus with varying angle relationships, nystagmus, light sensitivity and substantial visual deficits. Finally a Kabuki syndrome could be confirmed by human genetic investigations (8q22-23 triplication).

Entities:  

Mesh:

Year:  2010        PMID: 20013277     DOI: 10.1007/s00347-009-2026-x

Source DB:  PubMed          Journal:  Ophthalmologe        ISSN: 0941-293X            Impact factor:   1.059


  3 in total

1.  Triplication of 8p22-8p23 in a patient with features similar to Kabuki syndrome.

Authors:  Joseph T C Shieh; Louanne Hudgins; Athena M Cherry; Zhezhong Shen; H Eugene Hoyme
Journal:  Am J Med Genet A       Date:  2006-01-15       Impact factor: 2.802

Review 2.  Kabuki make-up syndrome: a review.

Authors:  Naomichi Matsumoto; Norio Niikawa
Journal:  Am J Med Genet C Semin Med Genet       Date:  2003-02-15       Impact factor: 3.908

3.  The C20orf133 gene is disrupted in a patient with Kabuki syndrome.

Authors:  Nicole M C Maas; Tom Van de Putte; Cindy Melotte; Annick Francis; Constance T R M Schrander-Stumpel; Damien Sanlaville; David Genevieve; Stanislas Lyonnet; Boyan Dimitrov; Koenraad Devriendt; Jean-Pierre Fryns; Joris R Vermeesch
Journal:  J Med Genet       Date:  2007-06-23       Impact factor: 6.318

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.