Arthrogryposis multiplex congenita

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What is arthrogryposis multiplex congenita?

A rthrogryposis multiplex congenita is a rare genetic disorder in which affected individuals are born with one or more areas of a permanently fixed bending at the joints. A contracture is the word used to describe what happens at the joints to cause this bending.

Common symptoms reported by people with arthrogryposis multiplex congenita

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 arthrogryposis multiplex congenita

No data

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Compare treatments taken by people with arthrogryposis multiplex congenita

No data

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Who has arthrogryposis multiplex congenita on PatientsLikeMe?


Age
Age Proportion # of patients
<20 0
20s 0
30s 1
40s 0
50s 0
60s 0
70+ 0
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 arthrogryposis multiplex congenita 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 arthrogryposis multiplex congenita through your profile, those stories and data appear here too.

Got a question about living with arthrogryposis multiplex congenita? Members in the forum might have the answers.