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Currently, how confident are you in your ability to:
1 = not confident, 2 = somewhat confident, 3 = confident, 4 = very confident, 5 = extremely confident, N/A = not applicable to me
Develop personalized treatment plans for patients with spinal muscular atrophy
Apply clinical trial data when managing patients with spinal muscular atrophy
Indicate how often you CURRENTLY use the following clinical practice strategy for your patients with spinal muscular atrophy.
*1 = Never, 2 = Not often, 3 = Sometimes, 4 = Often, 5 = Always, N/A = Not applicable to me
Analyze the pathology, biology and molecular genetics of spinal muscular atrophy when treating SMA patients.
1. A couple undergoes prenatal carrier screening via qPCR and one is positive and the other is negative for SMA carrier status. Based on this result, they would be counseled that their risk of having a child with SMA is:
2. The most commonly diagnosed type of Spinal Muscular Atrophy (i.e. most incident form) is:
3. Except in very severe forms, Survival Motor Neuron protein deficiency does not compromise: