WebJul 24, 2024 · Congenital femoral deficiency represents a dysplastic phenomenon that involves a broad spectrum of femoral involvement ranging from the short hypoplastic femur to the complete absence of proximal femur. This dysplasia leads to abnormal gait, impaired childhood growth, psychosocial, behavioral changes, and cosmetic implications. [6] WebJan 25, 2024 · Several different classification systems exist for postaxial polydactyly of the hands, including the (a) Pritsch, (b) Rayan and Al-Qattan, and (c) Duran classification systems. Duran et al. introduced their new classification system for post-axial polydactyly in 2015 6. This new classification was created as it was felt that the current systems ...
Congenital Femoral Deficiency Article
WebJul 1, 2014 · Proximal focal femoral deficiency (FPPD), which is present in our patient, is a rare developmental disorder of the proximal femur that results in failure of formation or differentiation of the proximal femur and associated acetabulum. Its association with fibular a/hypoplasia is reported in approximately 50% of cases [15]. WebAug 2, 2024 · Ulnar dimelia or mirror hand syndrome is a rare congenital anomaly of the upper limb characterized by absence of the radial ray (including thumb), duplication of the ulna and duplication of the ulnar halves of the carpals, metacarpals and phalanges 1. On this page: Article: Pathology; Radiographic features; Treatment; grappling moves list
Proximal femoral focal deficiency – a rare congenital entity: two …
WebNov 4, 2009 · This disorder of the femurs has been called PFFD (proximal focal femoral deficiency) in this country ( Aitken, 1969) and is probably heterogeneous. Lenz (1977) … WebApr 5, 2024 · Preaxial polydactyly is less common than postaxial polydactyly, with an estimated incidence of 1 in 7000. Associations Preaxial polydactyly may be associated with: Down syndrome VATER association Holt-Oram syndrome Greig cephalopolysyndactyly syndrome Carpenter syndrome Laurin-Sandrow syndrome Fanconi anemia References WebJan 18, 2024 · Fibular hemimelia is a congenital lower limb anomaly characterized by partial or complete absence of the fibula and includes a spectrum ranging from mild fibular hypoplasia to complete fibular aplasia 1. Epidemiology Although rare in occurrence, it is the most common congenital absence of long bone of the extremities 2. chithi 2 replacement