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The genetic basis of alopecia areata: HLA associations with patchy alopecia areata versus alopecia totalis and alopecia universalis

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Clinical features include weight loss, dystonia, stunted growth, and epilepsy, with an epilepsy incidence of 33.3%, most commonly presenting as generalized tonicclonic and myoclonic seizures ( SCO2 mutations tend to have earlier-onset symptoms that progress more rapidly, including hypertrophic cardiomyopathy, dystonia, and seizures

While each component stands fully capable of supporting normal cellular function on its own, our research strongly suggests that the proper ratio found in Profaya yields a greater result than the sum of its parts