Literature DB >> 7949642

Partial DiGeorge syndrome at the age of thirty-four.

A Hirotani1, S Morimoto, E Koh, T Ogihara.   

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.

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Year:  1994        PMID: 7949642     DOI: 10.2169/internalmedicine.33.418

Source DB:  PubMed          Journal:  Intern Med        ISSN: 0918-2918            Impact factor:   1.271


  4 in total

1.  Characteristics of 22q 11.2 deletion syndrome undiagnosed until adulthood: an example suggesting the importance of psychiatric manifestations.

Authors:  Kenta Furuya; Yosuke Sasaki; Taizo Takeuchi; Yoshihisa Urita
Journal:  BMJ Case Rep       Date:  2015-06-08

2.  Di-George syndrome presenting with hypocalcaemia in adulthood: two case reports and a review.

Authors:  P S Kar; B Ogoe; R Poole; D Meeking
Journal:  J Clin Pathol       Date:  2005-06       Impact factor: 3.411

3.  Neuropsychiatric aspects of 22q11.2 deletion syndrome: considerations in the prenatal setting.

Authors:  Anne S Bassett; Gregory Costain; Christian R Marshall
Journal:  Prenat Diagn       Date:  2016-11-14       Impact factor: 3.050

4.  An Adult Case of Chromosome 22q11.2 Deletion Syndrome Associated with a High-positioned Right Aortic Arch.

Authors:  Yoichi Hoshino; Moriya Machida; Shun-Ichi Shimano; Teizo Taya
Journal:  Intern Med       Date:  2017-04-01       Impact factor: 1.271

  4 in total

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