This table lists symptoms that people with this disease may have. For most diseases, symptoms will vary from person to person. People with the same disease may not have all the symptoms listed. This information comes from a database called the Human Phenotype Ontology (HPO) . The HPO collects information on symptoms that have been described in medical resources. The HPO is updated regularly. Use the HPO ID to access more in-depth information about a symptom.
| Medical Terms | Other Names | Learn More: HPO ID |
|---|---|---|
| 80%-99% of people have these symptoms | ||
| Gait disturbance |
Abnormal gait
Abnormal walk
Impaired gait
[ more ]
|
0001288 |
| Joint stiffness |
Stiff joint
Stiff joints
[ more ]
|
0001387 |
| Methylmalonic acidemia | 0002912 | |
|
Decreased body height
Small stature
[ more ]
|
0004322 | |
| 30%-79% of people have these symptoms | ||
| Abnormality of the knee | 0002815 | |
| Enlarged interphalangeal joints |
Enlarged hinge joints
|
0006247 |
| Flattened epiphysis |
Flat end part of bone
|
0003071 |
| Kyphosis |
Hunched back
Round back
[ more ]
|
0002808 |
| Osteoarthritis |
Degenerative joint disease
|
0002758 |
| Sclerotic vertebral endplates | 0004576 | |
| 0002650 | ||
| Percent of people who have these symptoms is not available through HPO | ||
| Abnormality of the foot |
Abnormal feet morphology
Abnormality of the feet
Foot deformities
Foot deformity
[ more ]
|
0001760 |
| Arthropathy |
Disease of the joints
|
0003040 |
| 0000007 | ||
| Camptodactyly of finger |
Permanent flexion of the finger
|
0100490 |
| Coxa vara | 0002812 | |
| Decreased cervical spine mobility |
Limited neck movement
|
0004637 |
| Difficulty walking |
Difficulty in walking
|
0002355 |
| Enlarged epiphyses |
Large end part of bone
|
0010580 |
| Enlarged metacarpophalangeal joints | 0006163 | |
| Enlargement of the proximal femoral epiphysis |
Enlarged end part of innermost thighbone
|
0003371 |
| Genu varum |
Outward bow-leggedness
Outward bowing at knees
[ more ]
|
0002970 |
| Joint swelling | 0001386 | |
| Kyphoscoliosis | 0002751 | |
| Metaphyseal widening |
Broad wide portion of long bone
|
0003016 |
| Muscle weakness |
Muscular weakness
|
0001324 |
| 0000939 | ||
| Platyspondyly |
Flattened vertebrae
|
0000926 |
| Waddling gait |
'Waddling' gait
Waddling walk
[ more ]
|
0002515 |
Making a diagnosis for a genetic or rare disease can often be challenging. Healthcare professionals typically look at a person’s medical history, symptoms, physical exam, and laboratory test results in order to make a diagnosis. The following resources provide information relating to diagnosis and testing for this condition. If you have questions about getting a diagnosis, you should contact a healthcare professional.
If you need medical advice, you can look for doctors or other healthcare professionals who have experience with this disease. You may find these specialists through advocacy organizations, clinical trials, or articles published in medical journals. You may also want to contact a university or tertiary medical center in your area, because these centers tend to see more complex cases and have the latest technology and treatments.
If you can’t find a specialist in your local area, try contacting national or international specialists. They may be able to refer you to someone they know through conferences or research efforts. Some specialists may be willing to consult with you or your local doctors over the phone or by email if you can't travel to them for care.
You can find more tips in our guide, How to Find a Disease Specialist. We also encourage you to explore the rest of this page to find resources that can help you find specialists.
Related diseases are conditions that have similar signs and symptoms. A health care provider may consider these conditions in the table below when making a diagnosis. Please note that the table may not include all the possible conditions related to this disease.
|
Conditions with similar signs and symptoms from Orphanet
|
|---|
|
PPAC can be initially misdiagnosed as juvenile rheumatoid arthritis but is distinguished on radiographic analysis (especially the platyspondyly and generalised epiphyseal dysplasia) and the absence of inflammatory joint disease. PPAC must be differentiated from juvenile idiopathic arthritis to ensure optimal treatment and to avoid unnecessary exposure to immunosuppressants.
Visit the
Orphanet disease page
for more information.
|
Research helps us better understand diseases and can lead to advances in diagnosis and treatment. This section provides resources to help you learn about medical research and ways to get involved.
Support and advocacy groups can help you connect with other patients and families, and they can provide valuable services. Many develop patient-centered information and are the driving force behind research for better treatments and possible cures. They can direct you to research, resources, and services. Many organizations also have experts who serve as medical advisors or provide lists of doctors/clinics. Visit the group’s website or contact them to learn about the services they offer. Inclusion on this list is not an endorsement by GARD.
These resources provide more information about this condition or associated symptoms. The in-depth resources contain medical and scientific language that may be hard to understand. You may want to review these resources with a medical professional.
Questions sent to GARD may be posted here if the information could be helpful to others. We remove all identifying information when posting a question to protect your privacy. If you do not want your question posted, please let us know.
