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ABGC 100 Genetic Conditions | Q&A Latest Update 2024/2025 | 100% PASS
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ABGC 100 Genetic Conditions | Q&A Latest Update 2024/2025 | 100% PASS T13 - Answer -Nondisjunction; 1 in 12,000 SGA, MCA: hypotelorism, CLP, heart, brain and kidney defects RR is 1% T18 - Answer -Nondisjunction; 1 in 6,000 SGA, MCA: prominent occiput, tightly clenched fingers, heart and brain defects Choroid plexus cyst on u/s RR is 1% T21 - Answer -MATERNAL nondisjunction (90%); 5% translocation 21;**usually 14**; 2% mosaic T21 1 in 800 Hypotonic, heart (50%) and GI defects common Mild to moderate ID Immunodeficiency, leukemia common Adults at risk for EO-AZD RR is 1%; Robertsonian ~15-100
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