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: | , , , , , |
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Format: | Article |
Language: | English |
Published: |
Serbian Medical Society
2011-01-01
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Series: | Srpski Arhiv za Celokupno Lekarstvo |
Subjects: | |
Online Access: | http://www.doiserbia.nb.rs/img/doi/0370-8179/2011/0370-81791110681P.pdf |