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Partial DiGeorge syndrome at the age of thirty-four
A Hirotani1, S Morimoto, E Koh
1Department of Geriatric Medicine, Osaka University Medical School.
Internal Medicine (Tokyo, Japan)
|July 1, 1994
Abstract:
A 34-year-old man with partial DiGeorge syndrome suffered from seizures and mental retardation from the age of three years. He was diagnosed as having primary hypoparathyroidism by the Ellsworth-Howard test at the age of 22. He was also found to have a right aortic arch. Immunological studies revealed the presence of immature T cells (CD 38+, OKT 9+), although the subsets and function of his T cells were almost normal. The facts that the cardiovascular anomaly and immunodeficiency were mild and the hypoparathyroidism was well controlled, may account for his survival to this age.