Search results
Results from the WOW.Com Content Network
Sinding-Larsen and Johansson syndrome, [1] named after Swedish surgeon Sven Christian Johansson (1880-1959), [2] and Christian Magnus Falsen Sinding-Larsen (1866-1930), [3] a Norwegian physician, is apophysitis of the inferior pole of the patella. It is analogous to Osgood–Schlatter disease which involves the upper margin of the tibia. This ...
Patients with Larsen syndrome normally present with a variety of symptoms, including congenital anterior dislocation of the knees, dislocation of the hips and elbows, flattened facial appearance, prominent foreheads, and depressed nasal bridges. [2] Larsen syndrome can also cause a variety of cardiovascular [3] and orthopedic abnormalities. [4]
Non-articular: This group includes Sever's disease (of the calcaneus, or heel), and other conditions not completely characteristic of the osteochondroses, such as Osgood-Schlatter's disease (of the tibial tubercle) [10] and Sinding-Larsen-Johansson syndrome (proximal patellar tendon).
Sinding-Larsen and Johansson syndrome, [16] is an analogous condition involving the patellar tendon and the lower margin of the patella bone, instead of the upper margin of the tibia. Sever's disease is an analogous condition affecting the Achilles tendon attachment to the heel. [citation needed]
He was born in Kristiania as a son of jurist and writer Alfred Sinding-Larsen (1839–1911) and Elisabeth Lange (1841–1887). [1] He was a brother of colonel Birger Fredrik Sinding-Larsen, architect Holger Sinding-Larsen and painter Kristofer Sinding-Larsen, and also a grandnephew of mining engineer Matthias Wilhelm Sinding, second cousin of painter Sigmund Sinding, [2] maternal great ...
Epiphysiodesis is a pediatric orthopedic surgery procedure that aims at altering or stopping the bone growth naturally occurring through the growth plate also known as the physeal plate. There are two types of epiphysiodesis: temporary hemiepiphysiodesis and permanent epiphysiodesis.
Lobstein syndrome; Madelung's deformity; Maffucci syndrome; Marfan syndrome; Marie-Strümpell disease; Marshall syndrome; Marshall–Smith syndrome; McCune–Albright syndrome; Melnick–Needles syndrome; Morton's toe; Ollier disease; Rett syndrome; Rubinstein–Taybi syndrome; Scheuermann's disease; Schwartz–Jampel syndrome; Silver–Russell ...
Bizarre parosteal osteochondromatous proliferation (BPOP), also known as Nora's lesion, [4] is a type of non-cancerous bone tumor belonging to the group of cartilage tumors. [1] [2] [5] It is generally seen in the tubular bones of the hands and feet, [6] where it presents with a rapidly enlarging painless lump in a finger or toe.