Femur-fibula-ulna syndrome, or FFU syndrome, is a very rare, sporadically occurring condition marked by combined malformations of the femur, or thigh bone, the fibula, or calf bone, and the ulna, one of the forearm bones. It affects multiple limbs at once, with the upper limbs typically showing more severe abnormalities than the lower limbs, and malformations occurring more often on the right side than the left, with no predictable pattern from one case to the next. It was first identified by Lenz and Feldman in 1977, and there remains ongoing medical debate over whether it is truly distinct from proximal femoral focal deficiency or represents the same underlying condition.
Facts
Classification
ICD-10 ChapterXVII: Congenital Malformations, Deformations and Chromosomal Abnormalities 2 Communicable or Non-communicable Transmission Route First Described Sources
1. Wikipedia: Femur fibula ulna syndrome
WikipediaArticle text
The condition was first noted by Lenz and Feldman in 1977.
Lead section, body-system statement
Femur-fibula-ulna syndrome (FFU syndrome) is a very rare syndrome characterized by abnormalities of the femur (thigh bone), fibula (calf bone) and the ulna (forearm bone).
View the Source 2. Wikipedia: ICD-10
WikipediaList of chapters, Chapter XVIIQuote, List of chapters, Chapter XVII
Congenital malformations, deformations and chromosomal abnormalities
View the Source 3. Wikipedia: Non-communicable disease
WikipediaLead section, transmission-route statement (inferred from disease-category)
Genetic disorders are caused by errors in genetic information that produce diseases in the affected people.
Inherited/genetic diseases section
Genetic disorders are caused by errors in genetic information that produce diseases in the affected people.
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