Literature DB >> 2429001

Zinsser-Cole-Engman syndrome (dyskeratosis congenita) with cataract--a rare association.

V Menon, A Kumar, L Verma.   

Abstract

A 26-year-old male patient with dermatological and systemic features suggestive of dyskeratosis congenita is reported with an unusual associated ocular feature of bilateral cataract.

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Year:  1986        PMID： 2429001

Source DB:  PubMed          Journal:  Jpn J Ophthalmol        ISSN： 0021-5155            Impact factor:   2.447


  3 in total

1.  Enhanced G2 chromatid radiosensitivity in dyskeratosis congenita fibroblasts.

Authors:  D M DeBauche; G S Pai; W S Stanley
Journal:  Am J Hum Genet       Date:  1990-02       Impact factor: 11.025

Review 2.  Ocular involvement in primary immunodeficiency diseases.

Authors:  Sima Hosseinverdi; Hassan Hashemi; Asghar Aghamohammadi; Hans D Ochs; Nima Rezaei
Journal:  J Clin Immunol       Date:  2013-11-30       Impact factor: 8.542

Review 3.  Fanconi anemia and dyskeratosis congenita/telomere biology disorders: Two inherited bone marrow failure syndromes with genomic instability.

Authors:  Moisés Ó Fiesco-Roa; Benilde García-de Teresa; Paula Leal-Anaya; Renée van 't Hek; Talia Wegman-Ostrosky; Sara Frías; Alfredo Rodríguez
Journal:  Front Oncol       Date:  2022-08-25       Impact factor: 5.738
  3 in total

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