A rare primary bone dysplasia characterized by the association of multiple epiphyseal dysplasia, visual impairment (with early-onset progressive myopia, retinal thinning, and cataracts), and conductive hearing loss. Patients are of short stature and present brachydactyly, genu valgus deformity, and joint pain. [from ORDO]
- MedGen UID:
- 377049
- •Concept ID:
- C1851536
- •
- Disease or Syndrome