Digeorge syndrome: A case report
Introduction. DiGeorge syndrome is a genetic disorder caused by deletion of chromosome 22. The main features are congenital heart disease, absence or hypoplasia of thymus (with consecutive immunodeficiency and infections), hypoparathyroidism with consecutive hypocalcaemia, gastrointestinal proble...
Main Authors: | Popović-Deušić Smiljka, Lečić-Toševski Dušica, Pejović-Milovančević Milica, Draganić-Gajić Saveta, Aleksić-Hil Olivera, Radosavljev-Kirćanski Jelena |
---|---|
Format: | Article |
Language: | English |
Published: |
Serbian Medical Society
2011-01-01
|
Series: | Srpski Arhiv za Celokupno Lekarstvo |
Subjects: | |
Online Access: | http://www.doiserbia.nb.rs/img/doi/0370-8179/2011/0370-81791110681P.pdf |
Similar Items
-
Features of Diagnosing and Managing a Patient with DiGeorge Syndrome
by: O.S. Koreniuk, et al.
Published: (2016-04-01) -
Adjustment disorders in hospital treated adolescents: A follow-up study
by: Popović-Deušić Smiljka, et al.
Published: (2012-01-01) -
Follicular Helper T Cells in DiGeorge Syndrome
by: Adam Klocperk, et al.
Published: (2018-07-01) -
Psychotic spectrum disorders in childhood
by: Popović-Deušić Smiljka, et al.
Published: (2008-01-01) -
Palatoschisis, Schizophrenia and Hypocalcaemia: Phenotypic Expression of 22q11.2 Deletion Syndrome (DiGeorge Syndrome) in an Adult
by: Melissa Elise van der Meijs, et al.
Published: (2021-04-01)