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Mueller-Weiss syndrome

Diseases of the Musculoskeletal System and Connective Tissue

Mueller-Weiss syndrome, also called Mueller-Weiss disease, is a rare, idiopathic degenerative disease of the adult navicular bone in the foot, marked by progressive collapse and fragmentation of the bone that leads to pain and deformity of the mid- and hindfoot. It is seen mostly in women aged 40 to 60. Imaging characteristically shows lateral collapse of the navicular bone, and the condition was historically understood as a form of adult onset osteonecrosis caused by disrupted blood flow to the bone. Onset is sub-acute, often beginning as discomfort with prolonged standing that can progress to disabling pain; because symptoms can be out of proportion to visible signs, early diagnosis can be difficult. Pain is centered on the midfoot and hindfoot, and severe cases can include hindfoot varus deformity and flattening of the arch. Treatment falls under orthopedics and ranges from medication to surgery.

Facts
Classification
Body System
Skeletal System 1
Communicable or Non-communicable
Non-Communicable 1
First Described
1927 1
Sources
1. Mueller-Weiss syndrome (Wikipedia)
  • Lead: disease category
    Mueller-Weiss syndrome, also known as Mueller-Weiss disease, is a rare idiopathic degenerative disease of the adult navicular bone characterized by progressive collapse and fragmentation, leading to mid- and hindfoot pain and deformity.
  • Article text
    degenerative disease of the adult navicular bone
  • History section
    In 1927 Walther Mueller, a Leipzig orthopedic surgeon, reported a case that had severe damage to the navicular bone with compression and fragmentation.I have recently had occasion to observe changes in the os naviculare pedis in the adult, which may have some similarities with the Köhler-like disease of the adolescents, which is not yet known in this form.
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Mueller-Weiss syndrome (Wikipedia)
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