Dyskeratosis congenita: Difference between revisions
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==Case Studies== | ==Case Studies== | ||
[[Dyskeratosis congenita case study one|Case #1]] | [[Dyskeratosis congenita case study one|Case #1]] | ||
==External Links== | ==External Links== |
Revision as of 18:29, 6 June 2013
Dyskeratosis congenita Microchapters |
Diagnosis |
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Treatment |
Case Studies |
Dyskeratosis congenita On the Web |
American Roentgen Ray Society Images of Dyskeratosis congenita |
Risk calculators and risk factors for Dyskeratosis congenita |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Raviteja Guddeti, M.B.B.S. [2]
Synonyms and keywords: Zinsser-Cole-Engman syndrome; X-linked dyskeratosis congenita; Cole-Rauschkolb-Toomey syndrome; DKCX
Overview
Historical Perspective
Classification
Pathophysiology
Causes
Differentiating Dyskeratosis Congenita from other Diseases
Epidemiology and Demographics
Risk Factors
Screening
Natural History, Complications and Prognosis
Diagnosis
History and Symptoms | Physical Examination | Laboratory Findings | Electrocardiogram | X Ray | CT | MRI | Echocardiography or Ultrasound | Other Imaging Findings | Other Diagnostic Studies
Treatment
Medical Therapy | Surgery | Primary Prevention | Secondary Prevention | Cost-Effectiveness of Therapy | Future or Invesetigational Therapies
Case Studies
External Links
Template:Congenital malformations and deformations of integument Template:X-linked disorders