Abstract

Muller-Weiss sickness, otherwise called Müller-Weiss disorder or connective corruption of the tarsal navicular, is an uncommon foot condition described by unconstrained breakdown of the tarsal navicular bone in the midfoot. The disease mostly affects adults, usually in their fourth to sixth decade of life, and women are more likely than men to develop it. The pathogenesis of Müller-Weiss infection isn't completely perceived, however it is accepted to include a mix of mechanical, hereditary, and vascular elements. The tarsal navicular bone goes through connective rot, prompting distortion and breakdown. Patients frequently present with midfoot torment, expanding, and an adaptable gumshoe disfigurement. Determination is regularly affirmed through imaging studies, for example, X-beams and attractive reverberation imaging (X-ray). Treatment choices for Müller-Weiss sickness differ contingent upon the seriousness of side effects and the phase of the condition. Orthotic devices, physical therapy, and pain management are some conservative measures. In further developed cases, careful mediation, for example, arthrodesis or navicular bone extraction might be considered to address distortion and assuage torment.