Tyrosine hydroxylase deficiency

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What is tyrosine hydroxylase deficiency?

Tyrosine hydroxylase deficiency is a rare inherited disorder that is caused by a mutation in the TH gene. Affecting the nervous system, common symptoms may include lack of coordination when walking, unusual limb positioning, and involuntary movements of limbs or eyes.

Common symptoms reported by people with tyrosine hydroxylase deficiency

Common symptoms
How bad it is
What people are taking for it

Reports may be affected by other conditions and/or medication side effects. We ask about general symptoms (anxious mood, depressed mood, fatigue, pain, and stress) regardless of condition.
Last updated:

Treatments taken by people with tyrosine hydroxylase deficiency

No data

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Compare treatments taken by people with tyrosine hydroxylase deficiency

No data

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Got a question about living with tyrosine hydroxylase deficiency? Members in the forum might have the answers.

Who has tyrosine hydroxylase deficiency on PatientsLikeMe?


Age at first symptom
Age at first symptom Proportion # of patients
0-19 years 0
20-29 years 0
30-39 years 0
40-49 years 0
50-59 years 0
60-69 years 0
70+ years 0

Distribution of sex

Sex
Sex Proportion # of patients
Male 0
Female 1

Diagnosis status
Diagnosis status Proportion # of patients
Diagnosed 0
Not Diagnosed 0

These charts show data from tyrosine hydroxylase deficiency patients who have completed their condition history
Last updated:
No data

Let’s build this page together! When you share what it’s like to have tyrosine hydroxylase deficiency through your profile, those stories and data appear here too.

Got a question about living with tyrosine hydroxylase deficiency? Members in the forum might have the answers.