Complete Trisomy 21 Syndrome
specificA chromosomal dysgenesis syndrome resulting from a triplication or translocation of chromosome 21. This condition is characterized by distinctive facial and physical features: short stature, developmental delay, cardiac defects (atrioventricular septal defect, tetralogy of Fallot), hypo- and hyperthyroidism, autoimmune disease (type 1 diabetes mellitus), and hypogonadism.
Top Centers for Complete Trisomy 21 Syndrome
Ranked by research excellence score (trials · grants · publications). Methodology →
No centers currently specializing in this cancer type.
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