DiGeorge Sequence
DiGeorge Sequence Causes
DGS is caused by a genetic defect in the chromosome 22q11.
DiGeorge Sequence Definition
DiGeorge sequence (DGS), is an abnormal developmental condition that involves the third and fourth pharyngeal pouches.
DiGeorge Sequence Diagnosis
The disease can be diagnosed through molecular analysis of the affected genes.
DiGeorge Sequence Symptoms and Signs
DGS features certain defects such as hypo and aplasia conditions of the thymus and parathyroid glands. Congenital heart problems are also found, as well as facial dysmorphism.
DiGeorge Sequence Treatment
There is no specific treatment yet found for the disease.