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"The numbers are small, which is a challenge, but that's what happens with extraordinarily rare disorders."To avoid SIDS, infants and parents should share a room, report saysA mutation in the SCN4A gene has been linked to skeletal muscle disorders in adults. These disorders are typically characterized by an inability to effectively stimulate or relax skeletal muscles, resulting in excessive muscle stiffness or weakness.The shared genetic basis between these adult muscle disorders and some cases of SIDS could impact the screening and counseling of prospective parents with known skeletal muscle disorders, Cannon suggests."An interesting spin off to this study is whether the couple of thousand people who have these inherited muscle diseases in the United States should be advised and whether we should change the recommendations for how their infants are cared for," he said.However, Hanna cautioned that the mutation was found in only 1.4% of the infants who died of SIDS, meaning the vast majority of cases are still probably caused by a host of other factors. "I think it's probably a major factor, but it's not a sole factor," he said.

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