Tyrosinemia

Tyrosinemia or tyrosinaemia is an error of metabolism, usually inborn, in which the body cannot effectively break down the amino acid tyrosine. Symptoms of untreated tyrosinemia include liver and kidney disturbances. Without treatment, tyrosinemia leads to liver failure.[1] Today, tyrosinemia is increasingly detected on newborn screening tests before any symptoms appear. With early and lifelong management involving a low-protein diet, special protein formula, and sometimes medication, people with tyrosinemia develop normally, are healthy, and live normal lives.[2]

Tyrosinemia
Tyrosine
SpecialtyMedical genetics 

Cause
Tyrosinemia is inherited in an autosomal recessive pattern.

All tyrosinemias result from dysfunction of various genes in the phenylalanine and tyrosine catabolic pathway, and are inherited in an autosomal-recessive pattern.[3]

Type I tyrosinemia results from a mutation in the FAH gene, which encodes the enzyme fumarylacetoacetase.[4] As a result of FAH deficiency, the substrate fumarylacetoacetate can accumulate in proximal renal tubular cells and hepatocytes, resulting in damage to the kidney and liver, respectively.[3]

Type II tyrosinemia results from a mutation in the TAT gene, which encodes the enzyme tyrosine aminotransferase.[4] As a result of TAT deficiency, the substrate tyrosine accumulates, causing ophthalmologic and dermatologic abnormalities.[3]

Type III tyrosinemia results from a mutation in the HPD gene, which encodes the enzyme 4-hydroxyphenylpyruvate dioxygenase.[4] Type III tyrosinemia is the rarest of the three conditions, with only a few cases ever reported.[5] Most of those cases have included intellectual disability and neurologic dysfunction.[3]

Diagnosis

Types

Type I tyrosinemia can be detected via blood tests for the presence of a fumarylacetoacetate metabolite, succinylacetone, which is considered a pathognomonic indicator for the disease.[6]

Type II tyrosinemia can be detected via the presence of significantly elevated plasma tyrosine levels, and the diagnosis can be confirmed by detection of a mutation in TAT in cultured fibroblasts.

Type III tyrosinemia can be diagnosed by detection of a mutation in HPD in cultured fibroblasts.[3]

Pathophysiology of metabolic disorders of tyrosine, resulting in elevated levels of tyrosine in blood.

Treatment

Treatment varies depending on the specific type; a low-protein diet combined with the use of a specially engineered formula to supply protein is required in most cases. Experience with nitisinone has shown it to be effective, especially when started within the first month of life, and it is now the standard course of treatment. It is a 4-hydroxyphenylpyruvate dioxygenase inhibitor indicated for the treatment of hereditary tyrosinemia type 1 (HT-1) in combination with dietary restriction of tyrosine and phenylalanine.[7] Liver transplant is indicated for patients with tyrosinemia type I who do not respond to nitisinone, as well as those with acute liver failure and hepatomas.[8]

See also

References
  1. Shaw K, Bachur R (2016). Fleisher & Ludwig's Textbook of Pediatric Emergency Medicine. Wolters Kluwer. ISBN 978-1451193954.
  2. Zea-Rey AV, Cruz-Camino H, Vazquez-Cantu DL, Gutiérrez-García VM, Santos-Guzmán J, Cantú-Reyna C (Nov 2017). "The Incidence of Transient Neonatal Tyrosinemia Within a Mexican Population". Journal of Inborn Errors of Metabolism. 5 (1): 1–4. doi:10.1177/2326409817744230. Retrieved 12 March 2019.
  3. Grompe M (2016-12-20). "Disorders of Tyrosine Metabolism". www.uptodate.com. Retrieved 2018-02-23.
  4. Nelson D, Cox M (2013). Lehninger Principles of Biochemistry (6th ed.). New York: WH Freeman and Co. p. 719. ISBN 978-1-4292-3414-6.
  5. Heylen E, Scherer G, Vincent MF, Marie S, Fischer J, Nassogne MC (November 2012). "Tyrosinemia Type III detected via neonatal screening: management and outcome". Molecular Genetics and Metabolism. 107 (3): 605–7. doi:10.1016/j.ymgme.2012.09.002. PMID 23036342.
  6. De Jesús VR, Adam BW, Mandel D, Cuthbert CD, Matern D (2014-09-01). "Succinylacetone as primary marker to detect tyrosinemia type I in newborns and its measurement by newborn screening programs". Molecular Genetics and Metabolism. 113 (1–2): 67–75. doi:10.1016/j.ymgme.2014.07.010. PMC 4533100. PMID 25066104.
  7. Swedish Orphan Biovitrum AB, Orfadin [package insert] (PDF), retrieved 2016-07-12
  8. Mieles LA, Esquivel CO, Van Thiel DH, Koneru B, Makowka L, Tzakis AG, Starzl TE (January 1990). "Liver transplantation for tyrosinemia. A review of 10 cases from the University of Pittsburgh". Digestive Diseases and Sciences. 35 (1): 153–7. doi:10.1007/BF01537237. PMC 2974306. PMID 2153069.
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