Majeed syndrome
MeSH: C537839ORPHA: 77297
Overview
Majeed syndrome is a rare genetic multisystemic disorder characterized by the triad of chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia, and variable transient inflammatory dermatosis
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with Majeed syndrome, sourced from HPO and Orphanet clinical annotations.
Weight lossFeverBone painOsteomyelitisArthralgiaMetaphyseal irregularityCachexiaCongenital hypoplastic anemiaHypochromic microcytic anemiaAbnormal bone marrow cell morphologyAbnormal inflammatory responsePapulePustuleEdemaAcneFailure to thriveSplenomegalyIncreased total leukocyte countHepatomegalyHeadacheMyalgiaIncreased bone mineral densitySynovitisProteinuriaFlexion contractureMalabsorptionPulmonary infiltratesIncreased susceptibility to fracturesMicroscopic hematuriaInflammatory abnormality of the skinCoughGlomerulopathy
Classification & Codes
MeSH Code
C537839Orphanet Code
ORPHA:77297Majeed syndrome
| MeSH | C537839 |
| Orphanet | ORPHA:77297 |
| Treatments | 0 drug(s) |
| Symptoms on record | 32 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO