X-ring Turner’s syndrome with combined immunodeficiency and selective gonadotropin defect
- 9 April 1989
- journal article
- case report
- Published by Springer Nature in Journal of Endocrinological Investigation
- Vol. 12 (4) , 257-263
- https://doi.org/10.1007/bf03349979
Abstract
A rare association of chromosomal, immunological and endocrine defects is described in a young woman with short stature, recurrent pulmonary infections and primary amenorrhea. Cytogenetic studies showed a 45, X karyotype in 65% of peripheral blood lymphocytes and 46,Xr(X) (p22q27) karyotype in the remaining 35%. Severe immunodeficiency was revealed by phenotypical and functional studies and a selective gonadotropin defect was disclosed by endocrinological investigations. An attempt is made to explain the coexistence of the three abnormal pictures.Keywords
This publication has 33 references indexed in Scilit:
- Turner syndrome patients with a ring X chromosomeClinical Genetics, 2008
- Isolated Gonadotrope Failure in the Polyglandular Autoimmune SyndromeNew England Journal of Medicine, 1985
- THE ASSOCIATION OF SERUM IgM AND IgG LEVELS WITH THE NUMBER OF X CHROMOSOMES IN PATIENTS WITH ABNORMAL NUMBER OF X CHROMOSOMESInternational Journal of Immunogenetics, 1982
- Monoclonal Antibodies Defining Distinctive Human T Cell Surface AntigensScience, 1979
- Four families with immunodeficiency and chromosome abnormalities.Archives of Disease in Childhood, 1979
- Regulation of Gonadotropin Secretion in Turner's SyndromeNew England Journal of Medicine, 1978
- Expression of a receptor for IgM by human T cells in vitroEuropean Journal of Immunology, 1975
- Receptors for IgG molecules on human lymphocytes forming spontaneous rosettes with sheep red cellsEuropean Journal of Immunology, 1975
- Identification, Enumeration, and Isolation of B and T Lymphocytes from Human Peripheral BloodScandinavian Journal of Immunology, 1974
- Deletion of the long arms of chromosome 18 (46,XX,18q-) associated with absence of IgA and hypothyroidism in an adult.Journal of Medical Genetics, 1972