SAPHO syndrome: Introduction
SAPHO syndrome: A rare disorder involving skin (acne, pustulosis), bone (hyperostosis, osteitis) and joint problems.
More detailed information about the symptoms,
causes, and treatments of SAPHO syndrome is available below.
Symptoms of SAPHO syndrome
See full list of 20
symptoms of SAPHO syndrome
Wrongly Diagnosed with SAPHO syndrome?
SAPHO syndrome: Related Patient Stories
SAPHO syndrome: Complications
Read more about complications of SAPHO syndrome.
Causes of SAPHO syndrome
Read more about causes of SAPHO syndrome.
Misdiagnosis and SAPHO syndrome
Psoriasis often undiagnosed cause of skin symptoms in children: Children who suffer
from the skin disorder called psoriasis can often go...read more »
Psoriatic arthritis often undiagnosed cause of joint conditions: Patients with the skin condition psoriasis
can also have the related arthritis subtype called "psoriatic arthritis".
This arthritic condition tends to be...read more »
Read more about Misdiagnosis and SAPHO syndrome
SAPHO syndrome: Research Doctors & Specialists
Research related physicians and medical specialists:
- Bone, Joint and Orthopedic Specialists:
- Skin Health Specialists (Dermatology):
- Arthritis & Joint Health Specialists (Rheumatology):
- more specialists...»
Other doctor, physician and specialist research services:
Evidence Based Medicine Research for SAPHO syndrome
Medical research articles related to SAPHO syndrome include:
Click here to find more evidence-based articles on the TRIP Database
SAPHO syndrome: Animations
More SAPHO syndrome animations & videos
Prognosis for SAPHO syndrome
Prognosis for SAPHO syndrome:
prolonged unpredictable course
More about prognosis of SAPHO syndrome
Research about SAPHO syndrome
Visit our research pages for current research about SAPHO syndrome treatments.
Statistics for SAPHO syndrome
SAPHO syndrome: Broader Related Topics
Types of SAPHO syndrome
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Definitions of SAPHO syndrome:
Syndrome consisting of synovitis, acne, palmoplantar pustulosis, hyperostosis, and osteitis (SAPHO). The most common site of the disease is the upper anterior chest wall, characterized by predominantly osteosclerotic lesions, hyperostosis, and arthritis of the adjacent joints. The association of sterile inflammatory bone lesions and neutrophilic skin eruptions is indicative of this syndrome.
- (Source - Diseases Database)
SAPHO syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that SAPHO syndrome, or a subtype of SAPHO syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list SAPHO syndrome as a "rare disease".
Source - Orphanet
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