22q11.2 deletion syndrome
| 22q11.2 deletion syndrome | |
| ICD-10 | D82.1 |
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| ICD-9 | 279.11, 758.32 |
| OMIM | 188400 |
| DiseasesDB | 3631 |
| MeSH | D004062 |
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22q11.2 deletion syndrome Microchapters |
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Differentiating 22q11.2 deletion syndrome from other Diseases |
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Diagnosis |
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22q11.2 deletion syndrome On the Web |
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American Roentgen Ray Society Images of 22q11.2 deletion syndrome |
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Risk calculators and risk factors for 22q11.2 deletion syndrome |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor-In-Chief: Cafer Zorkun, M.D., Ph.D. [2]
Synonyms and keywords: Velocardiofacial syndrome; Di George syndrome; Strong syndrome; third and fourth pharyngeal arch syndrome of Di George; CATCH phenotype; conotruncal anomaly face syndrome
Overview
Historical Perspective
Pathophysiology
Differentiating 22q11.2 deletion syndrome from Other Diseases
Epidemiology and Demographics
Risk Factors
Screening
Natural History, Complications and Prognosis
Diagnosis
History and Symptoms | Physical Examination | Laboratory Findings | Electrocardiogram | CT | MRI | Echocardiography | Other Imaging Findings | Other Diagnostic Studies
Treatment
Medical Therapy | Surgery | Primary Prevention | Secondary Prevention | Cost-Effectiveness of Therapy | Future or Investigational Therapies
See also
This article incorporates public domain text from The U.S. National Library of Medicine