RT Book, Section A1 Hay, Jr, William W. A1 Levin, Myron J. A1 Deterding, Robin R. A1 Abzug, Mark J. SR Print(0) ID 1145456065 T1 Tyrosinemia, Hereditary T2 Quick Medical Diagnosis & Treatment Pediatrics YR 2017 FD 2017 PB McGraw-Hill Education PP New York, NY SN 9781264257614 LK accesspediatrics.mhmedical.com/content.aspx?aid=1145456065 RD 2024/03/28 AB Consider in a child who has liver disease with or without accompanying renal disease or bone diseaseElevated urinary succinylacetone is diagnostic of type 1 tyrosinemiaType I tyrosinemia is an autosomal recessive condition caused by deficiency of fumarylacetoacetase