Autoimmune hyperthyroidism in two adolescents with DiGeorge/velocardiofacial syndrome (22q11 deletion)

European Journal of Pediatrics

Volumn 161, Issue 4, 2002, Pages 233-234

  Segni, Maria ^a   Zimmerman, Donald ^a  

^a MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; AUTOIMMUNE DISEASE; BLOOD; CASE REPORT; CHROMOSOME 22; DIGEORGE SYNDROME; FEMALE; GENE DELETION; GENETICS; HUMAN; HYPERTHYROIDISM; LETTER; MALE; ARTICLE; AUTOIMMUNITY; CHROMOSOME 22Q; CHROMOSOME DELETION; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE ASSOCIATION; DISEASE COURSE; DISEASE SEVERITY; HOSPITALIZATION; HYPERPARATHYROIDISM; PRIORITY JOURNAL; VELOCARDIOFACIAL SYNDROME;

ADOLESCENT; AUTOIMMUNE DISEASES; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; FEMALE; GENE DELETION; HUMANS; HYPERTHYROIDISM; MALE;

CALCITRIOL; CALCIUM CARBONATE; VITAMIN D;

EID: 0036009316     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00431-001-0900-x     Document Type: Article

References (6)

1. Clinical characteristics of children with hypoparathyroidism due to 22q11.2 microdeletion
2. DiGeorge syndrome: Long-term survival complicated by Graves disease
3. The DiGeorge sequence. II. Immunologic findings in partial and complete forms of the disorder
4. Immune hemolytic anemia, thrombocytopenia and liver disease in a patient with Di George syndrome
5. Lack of correlation between impaired T cell production, immunodeficiency, and other phenotypic features in chromosome 22q11 deletion syndromes (DiGeorge syndrome/Velocardiofacial syndrome)
6. Juvenile rheumatoid arthritis and del(22q11) syndrome: A non random association