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. Author manuscript; available in PMC: 2012 Jan 17.
Published in final edited form as: J Child Neurol. 2007 Aug;22(8):1019–1026. doi: 10.1177/0883073807305672

Table 5.

Genetic Knowledge of Parents of Children Affected With Spinal Muscular Atrophy (SMA)

Topics %
Parents who identify causative gene as SMN1 70
Parents who know SMN is on a chromosome 85
Parents who identify affected genotype 56
Parents who identify carrier genotype 73
Parents who identify recurrence risk 93
Parents who think genetic information is helpful 88
Parents who understand that a negative carrier test does not entirely rule out SMA recurrence 59
Parents who believe SMA can occur when both parents are carriers 99
Parents who believe SMA can occur when 1 parent is a carrier 27
Parents who believe SMA can occur with 0 carriers 68
Parents who infer a second child with SMA will have the same type as the firsta 63
Parents who perceive that SMN2 copy number predicts severity 77
Parents who know their child’s SMN2 copy number 51
a

Data refer only to type 2 families.