Literature DB >> 14360753

Dyskeratosis congenita with pigmentation, dystrophia unguium, and leucokeratosis oris; review of the known cases reported to date and discussion of the disease from various aspects.

H N COLE, J RAUSCHKOLB, J TOOMEY.   

Abstract

Entities:  

Keywords:  LEUKOPLAKIA; MOUTH/diseases; NAILS/diseases; PIGMENTATION; SKIN/abnormalities

Mesh:

Year:  1955        PMID: 14360753     DOI: 10.1001/archderm.1955.01540280027005

Source DB:  PubMed          Journal:  AMA Arch Derm        ISSN: 0096-5359


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  7 in total

1.  Ectodermal defect with skeletal abnormalities.

Authors:  H J WALLACE
Journal:  Proc R Soc Med       Date:  1958-09

2.  Inactivation of the tumor suppressor genes causing the hereditary syndromes predisposing to head and neck cancer via promoter hypermethylation in sporadic head and neck cancers.

Authors:  Ian M Smith; Suhail K Mithani; Wojciech K Mydlarz; Steven S Chang; Joseph A Califano
Journal:  ORL J Otorhinolaryngol Relat Spec       Date:  2010-03-24       Impact factor: 1.538

3.  Dyskeratosis congenita (Zinsser-Cole-Engman syndrome). An autopsy case presenting with rectal carcinoma, non-cirrhotic portal hypertension, and Pneumocystis carinii pneumonia.

Authors:  K Kawaguchi; H Sakamaki; Y Onozawa; M Koike
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1990

Review 4.  Dyskeratosis congenita: clinical features and genetic aspects. Report of a family and review of the literature.

Authors:  C Sirinavin; A A Trowbridge
Journal:  J Med Genet       Date:  1975-12       Impact factor: 6.318

Review 5.  An update on the biology and management of dyskeratosis congenita and related telomere biology disorders.

Authors:  Marena R Niewisch; Sharon A Savage
Journal:  Expert Rev Hematol       Date:  2019-09-10       Impact factor: 2.819

6.  Dyskeratosis congenita.

Authors:  Lorenzo Gitto; Robert Stoppacher; Timothy Eric Richardson; Serenella Serinelli
Journal:  Autops Case Rep       Date:  2020-09-02

7.  Dyskeratosis congenita: rare case report of Syria.

Authors:  Firas Hussein; Zainab Omar
Journal:  Oxf Med Case Reports       Date:  2021-11-25
  7 in total

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