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
Communicable or Non-communicable First Described 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.
View the SourceMueller-Weiss syndrome (Wikipedia)
Reader Challenges (0)
No disputes yet. Spotted an error or a better source? Open the first one.
Sign in to dispute this or suggest a correction.