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3% [5][6] Scoliosis (pl.: scolioses) is a condition in which a person's spine has an irregular curve. [2] The curve is usually S- or C-shaped over three dimensions. [2][7] In some, the degree of curve is stable, while in others, it increases over time. [3] Mild scoliosis does not typically cause problems, but more severe cases can affect ...
AIS is the most common form of idiopathic scoliosis, accounting for around 90% of all cases. [51][44] Adolescent Idiopathic Scoliosis affects between 1-4% of teenagers, [52][53] with treatment being required for only 0.25% of teenagers with the condition. An even smaller portion of individuals may die due to the severe curvature as well as the ...
X-ray image of an Idiopathic scoliosis. The neuromechanics of idiopathic scoliosis is about the changes in the bones, muscles and joints in cases of spinal deformity consisting of a lateral curvature scoliosis and a rotation of the vertebrae within the curve, that is not explained by either congenital vertebral abnormalities, or neuromuscular disorders such as muscular dystrophy.
The management of scoliosis is complex and is determined primarily by the type of scoliosis encountered: syndromic, congenital, neuromuscular, or idiopathic. [1] Treatment options for idiopathic scoliosis are determined in part by the severity of the curvature and skeletal maturity, which together help predict the likelihood of progression.
Other common features include fragile, elastic skin with easy bruising, hypotonia, kyphoscoliosis (kyphosis and scoliosis), and mild osteopenia. [5] Type-I collagen is usually affected. It is very rare, with about 30 cases reported. It is more severe than the hypermobility type. Variations in the genes COL1A1 and COL1A2 cause it. [33]
OI type III causes osteopenic bones that fracture very easily, sometimes even in utero, often leading to hundreds of fractures during a lifetime; [24] early scoliosis that progresses until puberty; dwarfism (a final adult height frequently less than 4 feet or 120 centimetres); loose joints; and possible respiratory problems due to low rib cage ...
Henry Turner. Turner syndrome (TS), also known as 45,X, or 45,X0, is a genetic disorder in which a the patient's cells have only one X chromosome or are partially missing an X chromosome (sex chromosome monosomy) leading to the complete or partial deletion of the pseudoautosomal regions (PAR1, PAR2) in the affected X chromosome. [2][6][7] Most ...
Lethal in males, with rare exceptions. Rett syndrome (RTT) is a genetic disorder that typically becomes apparent after 6–18 months of age and almost exclusively in females. [4] Symptoms include impairments in language and coordination, and repetitive movements. [4]
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