Literature DB >> 6601257

Dyskeratosis congenita: two examples of this multisystem disorder.

R Womer, J E Clark, P Wood, H Sabio, T E Kelly.   

Abstract

Two brothers with the X-linked disorder, dyskeratosis congenita, are described. They showed the dermatologic triad of reticular hyperpigmentation, dystrophic nails, and leukoplakia oris as well as the other major feature of this disorder, aplastic anemia. Less common features observed included prenatal and postnatal growth retardation, mental retardation, elevated immunoglobulin levels, and gastrointestinal hemorrhage from mucosal ulceration. Previously unreported findings were intracranial calcifications and nutmeg-like cirrhotic changes of the liver. These brothers demonstrated that skeletal changes and bony fragility may predate anemia or steroid therapy. Although a DNA repair defect is postulated as a possible primary defect, cytogenetic studies revealed no evidence of increased chromosomal breakage.

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Year:  1983        PMID: 6601257

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  17 in total

1.  Skewed X-chromosome inactivation in female carriers of dyskeratosis congenita.

Authors:  K Devriendt; G Matthijs; E Legius; E Schollen; D Blockmans; C van Geet; H Degreef; J J Cassiman; J P Fryns
Journal:  Am J Hum Genet       Date:  1997-03       Impact factor: 11.025

2.  Dyskeratosis Congenita Without Oral Involvement: A Rare Hereditary Disease.

Authors:  Fariba Iraji; Kioumars Jamshidi; Mohsen Pourazizi; Bahareh Abtahi-Naeini
Journal:  Oman Med J       Date:  2015-05

3.  Case report: gastric carcinoma as a complication of dyskeratosis congenita in an adolescent boy.

Authors:  K R Chatura; S Nadar; S Pulimood; D Mathai; M M Mathan
Journal:  Dig Dis Sci       Date:  1996-12       Impact factor: 3.199

4.  Avascular Necrosis of Head of Femur in Dyskeratosis Congenita - A Rare Presentation.

Authors:  Mukand Lal; Manoj Thakur; Sandeep Kashyap
Journal:  Indian J Hematol Blood Transfus       Date:  2015-02-07       Impact factor: 0.900

5.  Dyskeratosis congenita.

Authors:  H R Davidson; J M Connor
Journal:  J Med Genet       Date:  1988-12       Impact factor: 6.318

6.  Clastogen-induced fragility may differentiate pancytopenia of congenital dyskeratosis from Fanconi anaemia.

Authors:  A Schneider; U Mayer; E Gebhart; D Harms; J Gromball; U Glöckel; J D Beck
Journal:  Eur J Pediatr       Date:  1988-10       Impact factor: 3.183

Review 7.  Dyskeratosis congenita as a disorder of telomere maintenance.

Authors:  Nya D Nelson; Alison A Bertuch
Journal:  Mutat Res       Date:  2011-07-02       Impact factor: 2.433

8.  Ocular and orbital manifestations of the inherited bone marrow failure syndromes: Fanconi anemia and dyskeratosis congenita.

Authors:  Ekaterini T Tsilou; Neelam Giri; Sarah Weinstein; Christine Mueller; Sharon A Savage; Blanche P Alter
Journal:  Ophthalmology       Date:  2009-12-22       Impact factor: 12.079

9.  Dyskeratosis congenita- management and review of complications: a case report.

Authors:  Shivam Sinha; Vikas Trivedi; Arvind Krishna; Nidhi Rao
Journal:  Oman Med J       Date:  2013-07

10.  Enhancing a Wnt-Telomere Feedback Loop Restores Intestinal Stem Cell Function in a Human Organotypic Model of Dyskeratosis Congenita.

Authors:  Dong-Hun Woo; Qijun Chen; Ting-Lin B Yang; M Rebecca Glineburg; Carla Hoge; Nicolae A Leu; F Brad Johnson; Christopher J Lengner
Journal:  Cell Stem Cell       Date:  2016-08-18       Impact factor: 24.633

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