Galactosemia
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What is galactosemia?
Galactosemia is a disorder that affects how the body processes a simple sugar called galactose. There are several types of galactosemia each caused by mutations in a particular gene. Type I is the most common and most severe form. The condition is inherited in an autosomal recessive pattern.
Common symptoms reported by people with galactosemia
Treatments taken by people with galactosemia

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Compare treatments taken by people with galactosemia

Let’s build this page together! When you share what it’s like to have galactosemia through your profile, those stories and data appear here too.
Got a question about living with galactosemia? Members in the forum might have the answers.
Who has galactosemia on PatientsLikeMe?
- 6 patients have this condition
- 0 new patients joined this month
- 3 say galactosemia is their primary condition
Age | Proportion | # of patients |
---|---|---|
<20 | 0 | |
20s | 1 | |
30s | 1 | |
40s | 0 | |
50s | 0 | |
60s | 1 | |
70+ | 1 |
Age at first symptom | Proportion | # of patients |
---|---|---|
0-19 years | 1 | |
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 | Proportion | # of patients |
---|---|---|
Male | 1 | |
Female | 1 |
Diagnosis status | Proportion | # of patients |
---|---|---|
Diagnosed | 2 | |
Not Diagnosed | 1 |

Let’s build this page together! When you share what it’s like to have galactosemia through your profile, those stories and data appear here too.
Got a question about living with galactosemia? Members in the forum might have the answers.