CORONERS ACT, 1975 AS AMENDED

Discussion GA1 is an autosomal recessive disorder of lysine, hydrozylysine, and tryptophan metabolism, caused by glutaryl-CoA dehydrogenase deficiency1, 2, 5-7 (United States prevalence 1:50,000)6. GA1 commonly presents before age 18 months with sudden onset encephalopathy … ................
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