What is tyrosinemia type I?
Tyrosinemia is a genetic disorder characterized by elevated blood levels of the amino acid tyrosine, a building block of most proteins. Type I is is caused by a shortage of the enzyme fumarylacetoacetate hydrolase. Symptoms usually appear in the first few months of life.
How do members experience tyrosinemia type I?
Top 5 symptoms reported by people with tyrosinemia type I*
Common symptoms
How bad it is
What people are taking for it
Common symptom
Depressed mood
How bad it is
What people are taking for it
Nothing reported yet
Common symptom
Fatigue
How bad it is
What people are taking for it
Nothing reported yet
Common symptom
Stress
How bad it is
What people are taking for it
Nothing reported yet
*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.
Top treatments taken by people for tyrosinemia type I*
Who has tyrosinemia type I on PatientsLikeMe?
| Age | Proportion | # of patients |
|---|---|---|
| <20 | 2 | |
| 20s | 3 | |
| 30s | 10 | |
| 40s | 3 | |
| 50s | 0 | |
| 60s | 1 | |
| 70+ | 2 |
Distribution of sex
| Sex | Proportion | # of patients |
|---|---|---|
| Male | 11 | |
| Female | 10 |