CRMO Awareness

Dr. Polly Ferguson is a Pediatric Rheumatologist that helps people of all ages, infant to 90 years old. If you have CRMO or even think you have it she will look over your information, your medical record and if she thinks it's a possibility she will see you. She is one of the most inspirational doctors that many say they have ever met in their lives. 
CRMO is a bone disease that affect mostly children but there are plenty of adults that are unfortunately affected too. This disease is found mostly in girls (5-1 ratio, girls-boys) CRMO is also a 1 in a million disease. Here is a little more info on the disease.
Chronic Recurrent Multifocal Osteomyelitis is an autoinflammatory disease that mostly affects children. The causes of the disease have been linked to gene mutations in some cases, especially on chromosome18q in one family. More research is needed on the genetic causes of this challenging condition. 

CRMO presents in patients with periodic fevers, bone pain and bone lesions that can develop anywhere in the body. This is a rare disease, that has been found to affect more girls than boys. The peak for symptom incidence is around 10 years of age, but symptoms can be present from toddler or preschool age to even when patients are on middle age or older. Some patients can have many affected areas in their body, or only a few sites in their body. 

Children will develop deep aching pain, limping, tenderness over affected areas and often fevers. Common sites are the long bones of the body, the collar bone (clavicle) and shoulder girdle. The spine, ankles and feet may also be affected. 

Patients may also present with skin manifestations, such as psoriasis, acne, or pustules on the hands and feet. Some patients may also have uveitis, or inflammatory bowel disease along with CRMO symptoms. Another autoinflammatory disease, Majeed, involves CRMO, but also presents with symptoms of congenital dyserythropoietic anemia and Sweet Syndrome. Majeed is linked to an autosomal recessive inheritance of an LPIN2 gene mutation from both parents, and is a very rare disease. 

Please go to this site for more detailed information on CRMO at this link:http://www.bonetumor.org/tumors-unknown-type/chronic-recurrent-multifocal-osteomyelitis-crmo