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Second & Third Trimesters - Module 5: Genetic Abnormalities

This module begins with a discussion of autosomal recessive and autosomal dominant disorders and X-linked abnormalities. The sonographic presentation and markers of common genetic abnormalities such as Trisomy 13 (Patau Syndrome), Trisomy 18 (Edwards Syndrome), Trisomy 21 (Down Syndrome), and Turner Syndrome are presented. Nonaneuploidic syndromes, associations, and sequences covered include amniotic band, BeckwithWiedemann, caudal regression, sirenomelia, Mecker Gruber and Ellis van Creveld syndromes. In conclusion, Jim Baun BS, RDMS, RVT, FSDMS presents congenital anomalies with VACTERL and CHARGE association.

Viewing Time: 25 min
Customized Review: 19 min

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CME: This activity is approved for 0.75 SDMS CME (These credits are ARDMS-accepted CME credits.)

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