DiGeorge Syndrome

Congenital syndrome characterized by a wide spectrum of characteristics including the absence of the THYMUS and PARATHYROID GLANDS resulting in T-cell immunodeficiency, HYPOCALCEMIA, defects in the outflow tract of the heart, and craniofacial anomalies.

Also Known As:

Syndrome, DiGeorge; Velocardiofacial Syndrome; 22q11.2 Deletion Syndrome; 22q11.2DS; Autosomal Dominant Opitz G-Bbb Syndrome; Catch22; Conotruncal Anomaly Face Syndrome; Conotruncal Anomaly Face Syndrome (CTAF); Deletion 22q11.2 Syndrome; DiGeorge Anomaly; DiGeorge Sequence; Familial Third and Fourth Pharyngeal Pouch Syndrome; Hypoplasia of Thymus and Parathyroids; Pharyngeal Pouch Syndrome; Sedlackova Syndrome; Shprintzen Syndrome; Shprintzen VCF Syndrome; Third and Fourth Pharyngeal Pouch Syndrome; Thymic Aplasia Syndrome; VCF Syndrome; Velo-Cardio-Facial Syndrome; Autosomal Dominant Opitz G Bbb Syndrome; Deletion Syndrome, 22q11.2; Syndrome, Sedlackova; Syndrome, Shprintzen; Syndrome, VCF; Syndrome, Velo-Cardio-Facial; Syndrome, Velocardiofacial; Velo Cardio Facial Syndrome

Musculoskeletal Diseases: 719
- Musculoskeletal Abnormalities: 43
  - Craniofacial Abnormalities: 203
    - 22q11 Deletion Syndrome: 43
      - DiGeorge Syndrome: 680
Cardiovascular Diseases: 91362
- Heart Diseases: 26014
  - Congenital Heart Defects: 8917
    - 22q11 Deletion Syndrome: 43
      - DiGeorge Syndrome: 680
- Cardiovascular Abnormalities: 452
  - Congenital Heart Defects: 8917
    - 22q11 Deletion Syndrome: 43
      - DiGeorge Syndrome: 680
Hemic and Lymphatic Diseases: 6
- Lymphatic Diseases: 92
  - Lymphatic Abnormalities: 46
    - 22q11 Deletion Syndrome: 43
      - DiGeorge Syndrome: 680
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Congenital Abnormalities: 25723
  - Cardiovascular Abnormalities: 452
    - Congenital Heart Defects: 8917
      - 22q11 Deletion Syndrome: 43
        DiGeorge Syndrome: 680
  - Multiple Abnormalities: 211
    - 22q11 Deletion Syndrome: 43
      - DiGeorge Syndrome: 680
  - Chromosome Disorders: 136
    - 22q11 Deletion Syndrome: 43
      - DiGeorge Syndrome: 680
  - Lymphatic Abnormalities: 46
    - 22q11 Deletion Syndrome: 43
      - DiGeorge Syndrome: 680
  - Musculoskeletal Abnormalities: 43
    - Craniofacial Abnormalities: 203
      - 22q11 Deletion Syndrome: 43
        DiGeorge Syndrome: 680
- Inborn Genetic Diseases: 11939
  - Chromosome Disorders: 136
    - 22q11 Deletion Syndrome: 43
      - DiGeorge Syndrome: 680
Endocrine System Diseases: 968
- Parathyroid Diseases: 240
  - Hypoparathyroidism: 2755
    - 22q11 Deletion Syndrome: 43
      - DiGeorge Syndrome: 680

Deborah M Alcorn Selected Research

Deborah M Alcorn Research Topics

Disease

Drug/Important Bio-Agent (IBA)

Therapy/Procedure