Coffin-Lowry syndrome
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What is Coffin-Lowry syndrome?
Coffin-Lowry syndrome is a genetic condition characterized by head, facial, and bone abnormalities, developmental delay, short stature, and decreased muscle tone.
Common symptoms reported by people with Coffin-Lowry syndrome
Treatments taken by people with Coffin-Lowry syndrome
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Compare treatments taken by people with Coffin-Lowry syndrome
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Got a question about living with Coffin-Lowry syndrome? Members in the forum might have the answers.
Who has Coffin-Lowry syndrome on PatientsLikeMe?
- 8 patients have this condition
- 0 new patients joined this month
- 7 say Coffin-Lowry syndrome is their primary condition
| Age | Proportion | # of patients |
|---|---|---|
| <20 | 2 | |
| 20s | 1 | |
| 30s | 0 | |
| 40s | 2 | |
| 50s | 1 | |
| 60s | 0 | |
| 70+ | 0 |
| 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 | Proportion | # of patients |
|---|---|---|
| Male | 3 | |
| Female | 3 |
| Diagnosis status | Proportion | # of patients |
|---|---|---|
| Diagnosed | 0 | |
| Not Diagnosed | 0 |
Let’s build this page together! When you share what it’s like to have Coffin-Lowry syndrome through your profile, those stories and data appear here too.
Got a question about living with Coffin-Lowry syndrome? Members in the forum might have the answers.