Living with Arthrogryposis multiplex congenita
A physical finding in which several joints are stiff and fixed in position at birth, with many possible causes.
Understanding Arthrogryposis multiplex congenita
These joint contractures can limit movement and may lead to muscle wasting. AMC is not one specific diagnosis. It can go along with many different medical conditions. GARD says it is suspected to relate to less fetal movement before birth.
Signs & symptoms
GARD doesn't list specific symptoms for this condition, but its summary describes the main feature:
- Joints fixed in a bent or straight position (contractures)
- Joint contractures in two or more areas of the body
- Limited joint movement
- Muscle wasting in some people
Not everyone has every symptom. GARD's list comes from the Human Phenotype Ontology.
Diagnosis
- 1Talk with your doctor
Share the symptoms you've noticed, when they started and your family health history. Notes and photos can help.
- 2See a specialist
Specialists who may be involved include bone and joint specialists and genetic specialists.
- 3Ask which tests can help
Your care team will decide which exams and tests can confirm the diagnosis.
- 4Connect with expert centers
Arthrogryposis Multiplex Congenita Support Inc. may keep lists of experts for this condition.
Care & treatment
- Care team
- Bone and joint specialists (orthopedists or orthopedic surgeons); Genetic specialists (geneticists)
- Expert care
- Expert lists: Arthrogryposis Multiplex Congenita Support Inc.
- Treatment
- GARD doesn't list specific treatments for this condition. Your care team will tailor care to your symptoms.
- Research
- Clinical trials and observational studies may be options. See the research section below.
General information, not medical advice. Your care team makes the decisions.
Everyday life
Living with a rare condition is easier with support.
- Connect with Arthrogryposis Multiplex Congenita Support Inc.
- Keep notes on symptoms, changes and questions for appointments
- Ask about patient registries that help research
- Look into financial aid and travel resources for care visits
Quick facts
GARD says it may relate to less fetal movement, which can have many causes, including environmental factors (like maternal illness or limited space), single gene changes, chromosome differences, and various syndromes.
Also known as: amc; amc - arthrogryposis multiplex congenita; arthrogryposis multiplex; arthrogryposis, congenital; arthromyodysplasia congenita; congenital arthromyodysplasia
Patient organizations
- Arthrogryposis Multiplex Congenita Support Inc.Arthrogryposis multiplex congenita · United States
You are more than your diagnosis
Perspectives from people navigating life with Arthrogryposis multiplex congenita.
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