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] Ayushi Jain, M.B.B.S[3]
Synonyms and keywords: DiGeorge syndrome; 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
Classification
Pathophysiology
Differentiating 22q11.2 deletion syndrome from other Diseases
Causes
Epidemiology and Demographics
Risk Factors
Screening
Natural History, Complications and Prognosis
Diagnosis
History and Symptoms | Physical Examination | Laboratory Findings | Electrocardiogram | Chest X Ray | 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