Other Names for this Disease
- Chronic recurrent multifocal osteomyelitis, congenital
- Dyserythropoietic anemia, and neutrophilic dermatosis
- Congenital dyserythropoietic anemia and chronic recurrent multifocal osteomyelitis
- CDA and CRMO
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Majeed syndrome is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene. Although carriers typically do not show signs and symptoms of the condition, some parents of children with Majeed syndrome have had an inflammatory skin disorder called psoriasis.
Last updated: 10/31/2013
- Majeed syndrome. Genetics Home Reference (GHR). August 2009; http://ghr.nlm.nih.gov/condition/majeed-syndrome. Accessed 10/31/2013.