Carnitine palmitoyltransferase 2 deficiency
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What is Carnitine palmitoyltransferase 2 deficiency?
Carnitine palmitoyltransferase 2 deficiency is a mutation from the CPT2 gene, the body can not process certain fats for energy.
Common symptoms reported by people with Carnitine palmitoyltransferase 2 deficiency
Treatments taken by people with Carnitine palmitoyltransferase 2 deficiency
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Compare treatments taken by people with Carnitine palmitoyltransferase 2 deficiency
Let’s build this page together! When you share what it’s like to have Carnitine palmitoyltransferase 2 deficiency through your profile, those stories and data appear here too.
Got a question about living with Carnitine palmitoyltransferase 2 deficiency? Members in the forum might have the answers.
Who has Carnitine palmitoyltransferase 2 deficiency on PatientsLikeMe?
- 1 patients have this condition
- 0 new patients joined this month
- 1 say Carnitine palmitoyltransferase 2 deficiency is their primary condition
| Age | Proportion | # of patients |
|---|---|---|
| <20 | 0 | |
| 20s | 1 | |
| 30s | 0 | |
| 40s | 0 | |
| 50s | 0 | |
| 60s | 0 | |
| 70+ | 0 |
Distribution of sex
| Sex | Proportion | # of patients |
|---|---|---|
| Male | 0 | |
| Female | 1 |
Let’s build this page together! When you share what it’s like to have Carnitine palmitoyltransferase 2 deficiency through your profile, those stories and data appear here too.
Got a question about living with Carnitine palmitoyltransferase 2 deficiency? Members in the forum might have the answers.