Tyrosine hydroxylase deficiency
| Tyrosine hydroxylase deficiency | |
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| Simplified overview of the biosynthesis and catabolism of serotonin and the catecholamines, with tyrosine hydroxylase (TH) and its cofactor tetrahydrobiopterin (BH4) circled in red. Note that different parts of these processes take place in different tissues. Abbreviations: 3-MT, 3-methoxytyramine; 5-HTP, 5-hydroxytryptophan; 5HIAA, 5-hydroxyindolacetic acid; AAAHs, aromatic amino acid hydroxylases; AAAs, aromatic amino acids; AADC, aromatic acid decarboxylase; BH4, (6R)-L-erythro-5,6,7,8-tetrahydrobiopterin; COMT, catechol-O-methyltransferase; DBH, dopamine beta-hydroxylase; DOPAC, 3,4-dihydroxyphenylacetic acid; HVA, homovanillic acid; L-DOPA, L-3,4-dihydroxyphenylalanine; MN, metanephrine; MAO, monoamine oxidase; MPHG, 3-methoxy-4-hydroxyphenylethylene glycol; NMN, normetanephrine; PAH, phenylalanine hydroxylase; PLP, pyridoxal phosphate; PNMT, phenylethanolamine N-methyltransferase; TH, tyrosine hydroxylase; TPH, tryptophan hydroxylase. From a review by Gyrid Nygaard et al., 2021.[1] |
Tyrosine hydroxylase deficiency (THD) is a disorder caused by disfunction of tyrosine hydroxylase, an enzyme involved in the biosynthesis of dopamine. This condition is one of the causes of dopa-responsive dystonia.[2]
Symptoms and signs
[edit]Patients present with symptoms reflecting the decreased production of dopamine: hypokinetic-rigid syndrome, dystonia, complex encephalopathy. Symptom severity and age at onset are highly variable. A review published on GeneReviews and last updated in 2017 suggests the approximate subdivision of patients into three groups based on differences in severity of symptoms, nature of symptoms, and age at onset.[3] A review published more recently, in 2021, suggests that the disease may have a more gradual and overlapping spectrum, and categorization may be imprecise.[1]
According to the classification on GeneReviews,[3] three approximate phenotypes could be discerned:
- 1. TH-deficient dopa-responsive dystonia - the mildest phenotype with onset between 1 and 12 years of age, with its initial symptoms being lower-limb dystonia and/or difficulty in walking. Symptoms may gradually worsen over the day and become less pronounced after a period of rest.
- 2. TH-deficient infantile parkinsonism with motor delay - the intermediate phenotype, with onset between 3 and 12 months of age. Development of motor skills is visibly delayed, and trunkal hypotonia and parkinsonism are present.
- 3. TH-deficient progressive infantile encephalopathy - the most severe phenotype, with onset recognisable at the fetal stage of development. There is pronounced delay of motor development, truncal hypotonia, marked hypokinesia, limb hypertonia, hyperreflexia, oculogyric crises, ptosis, intellectual disability, and paroxysmal periods of lethargy (with increased sweating and drooling) alternating with irritability.
Cause
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Diagnosis
[edit]In order to diagnose tyrosine hydroxylase deficiency, a sample of the patient's cerebrospinal fluid may be obtained to assess neurotransmitter metabolites that may be affected, as illustrated by the metabolic links in Figure 1. Patients typically have normal levels of 5-hydroxyindolacetic acid (5HIAA), low levels of homovanillic acid (HVA) and 3-methoxy-4-hydroxyphenylethylene glycol (MHPG), and a low HVA:5-HIAA ratio.[1] Upon finding a pattern of CSF abrormalities suggestive of the disease, the diagnosis may be confirmed by analysing the TH gene encoding the enzyme.[1]
According to a review of dopa-responsive dystonias published in 2021, tyrosine hydroxylase deficiency may be hard to diagnose, with a median diagnostic delay of 4 years,[2] and misdiagnosis happens in a significant proportion of patients, with cerebral palsy being the most common erroneous diagnosis.[2]
Treatment
[edit]Patients with tyrosine hydroxylase deficiency are treated with L-dopa in conjunction with decarboxylase inhibitors. A significant percentage of patients do not achieve a complete response on this regimen.[1]
History
[edit]The first case reports of "Segawa syndrome" and parkinsonism caused by mutations in the tyrosine hydroxylase gene were published in 1995[1][4] and 1996.[5][6]
Alternative names
[edit]- Autosomal recessive Segawa syndrome (autosomal dominant Segawa syndrome affects a different gene, GCH1)
- DYT/PARK-TH - designation in accordance with the Nomenclature of Genetic Movement Disorders maintained by the International Parkinson and Movement Disorder Society[2]
- Dopa-responsive dystonia 5b, DYT5b
References
[edit]- ^ a b c d e f Nygaard G, Szigetvari PD, Grindheim AK, Ruoff P, Martinez A, Haavik J, Kleppe R, Flydal MI (November 2021). "Personalized Medicine to Improve Treatment of Dopa-Responsive Dystonia-A Focus on Tyrosine Hydroxylase Deficiency". Journal of Personalized Medicine. 11 (11): 1186. doi:10.3390/jpm11111186. PMC 8625014. PMID 34834538.
- ^ a b c d Weissbach A, Pauly MG, Herzog R, Hahn L, Halmans S, Hamami F, Bolte C, Camargos S, Jeon B, Kurian MA, Opladen T, Brüggemann N, Huppertz HJ, König IR, Klein C, Lohmann K (February 2022). "Relationship of Genotype, Phenotype, and Treatment in Dopa-Responsive Dystonia: MDSGene Review". Movement Disorders. 37 (2): 237–252. doi:10.1002/mds.28874. PMID 34908184. S2CID 245260405.
- ^ a b Adam, M. P.; Feldman, J.; Mirzaa, G. M.; Pagon, R. A.; Wallace, S. E.; Amemiya, A.; Furukawa, Y.; Kish, S. (1993). "Tyrosine Hydroxylase Deficiency". Tyrosine Hydroxylase Deficiency - GeneReviews® - NCBI Bookshelf. University of Washington, Seattle. PMID 20301610. Retrieved 20 June 2022.
- ^ Lüdecke B, Dworniczak B, Bartholomé K (January 1995). "A point mutation in the tyrosine hydroxylase gene associated with Segawa's syndrome". Human Genetics. 95 (1): 123–5. doi:10.1007/BF00225091. PMID 7814018. S2CID 26870241.
- ^ "Segawa syndrome, autosomal recessive; Online Mendelian Inheritance in Man (OMIM)". OMIM. 2022-06-20. Retrieved 2022-06-20.
- ^ Lüdecke B, Knappskog PM, Clayton PT, Surtees RA, Clelland JD, Heales SJ, Brand MP, Bartholomé K, Flatmark T (July 1996). "Recessively inherited L-DOPA-responsive parkinsonism in infancy caused by a point mutation (L205P) in the tyrosine hydroxylase gene". Human Molecular Genetics. 5 (7): 1023–8. doi:10.1093/hmg/5.7.1023. PMID 8817341.
External links
[edit]- Segawa syndrome, autosomal recessive- description in the OMIM compendium.