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. © 1994 The Japanese Society of Internal Medicine. All rights reserved.
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Hirotani, A., Morimoto, S., Koh, E., & Ogihara, T. (1994). Partial DiGeorge Syndrome at the Age of Thirty-Four. Internal Medicine, 33(7), 418–421. https://doi.org/10.2169/internalmedicine.33.418
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