Search results
Results from the WOW.Com Content Network
Diseases and disorders VACTERL-H Vertebral abnormalities, Anal atresia, Cardiac defects, Tracheoesophageal fistula, Esophageal atresia, Renal and radial abnormalities, Limb abnormalities with Hydrocephalus VAED Vaccine-associated enhanced disease VCFS Velo cardio facial syndrome: vCJD variant Creutzfeldt–Jakob disease: VD Venereal disease: VHF
SMA is a category of spinal disease that in linked with genetic disorders. More specifically, it is caused by an autosomal recessive disorder due to a homozygous mutation of a motor neuron gene. [3] There are different types of SMA. Type 0 is diagnosed to newborns who have muscle weakness, and little to no "fetal movements."
Spina bifida (SB; /ˌspaɪnə ˈbɪfɪdə/, [9] Latin for 'split spine') [10] is a birth defect in which there is incomplete closing of the spine and the membranes around the spinal cord during early development in pregnancy. [1] There are three main types: spina bifida occulta, meningocele and myelomeningocele. [1]
Diastematomyelia is a "dysraphic state" of unknown embryonic origin, but is probably initiated by an accessory neurenteric canal (an additional embryonic spinal canal.).) This condition may be an isolated phenomenon or may be associated with other segmental anomalies of the vertebral bodies such as spina bifida, kyphoscoliosis, butterfly vertebra, hemivertebra and block vertebrae which are ...
Jarcho–Levin syndrome associated with spina bifida and diastematomyelia (type I split cord malformation) 4: Duru S et al. 1999: 2: First case of 2-year-old girl, spondylocostal dysostosis with lipomyelomeningocele, and polythelia on the right side. Second case of 6-month-old girl, spondylocostal dysostosis with myelomeningocele and hydrocephalus
These include paraplegia, quadriplegia, muscular dystrophy, post-polio syndrome and spina bifida. [6] [footnotes 1] Minimal qualification for wheelchair sport is minimal body function impairment. In practice, ISMWSF has defined this as 70 points or less on the muscle group function test for people with lower limb and trunk impairments.
Body integrity dysphoria (BID), also referred to as body integrity identity disorder (BIID), amputee identity disorder or xenomelia, and formerly called apotemnophilia, is a rare mental disorder characterized by a desire to have a sensory or physical disability or feeling discomfort with being able-bodied, beginning in early adolescence and resulting in harmful consequences. [1]
Fibular hemimelia or longitudinal fibular deficiency is "the congenital absence of the fibula and it is the most common congenital absence of long bone of the extremities." [1] [2] It is the shortening of the fibula at birth, or the complete lack thereof.