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joint hypermobility การใช้

ประโยคมือถือ
  • Joint hypermobility syndrome is sometimes interchangeably called Ehlers Danlos syndrome hypermobile type.
  • However, people with " joint hypermobility syndrome " are subject to many difficulties.
  • People with Joint Hypermobility Syndrome may develop other conditions caused by their unstable joints.
  • Cervical joint hypermobility and defective internal jugular venous drainage have also been suggested as causes.
  • Joint hypermobility is a common symptom for both.
  • Joint hypermobility syndrome shares symptoms with other conditions such as Marfan syndrome, Ehlers-Danlos Syndrome, and osteogenesis imperfecta.
  • Patients taking anticoagulants, joint hypermobility and osteopenia should be given special consideration before articulatory techniques are employed.
  • Symptoms include gingival fibromatosis, associated with hypoplasia of the distal phalanges, nail dysplasia, joint hypermobility, and sometimes hepatosplenomegaly.
  • Given proper care, cats with feline cutaneous asthenia can live long lives, although the prognosis is not as positive if joint hypermobility is present.
  • Forms of EDS in this category may present with soft, mildly stretchable skin, shortened bones, chronic diarrhea, joint hypermobility and dislocation, bladder rupture, or poor wound healing.
  • When this condition affects joints in the entire body, it is called generalized joint hypermobility, which occurs in about five percent of the population, and may be genetic.
  • If considering surgical intervention, it would be prudent to seek care from a surgeon with extensive knowledge and experience in treating patients with EDS and joint hypermobility issues.
  • Proprioception is permanently impaired in patients that suffer from joint hypermobility or Ehlers-Danlos Syndrome ( a genetic condition that results in weak connective tissue throughout the body ).
  • In heritable connective tissue disorders associated with joint hypermobility ( such as Marfan syndrome and Ehlers-Danlos syndrome types I-III, VII, and XI ), the joint laxity usually is apparent before adulthood.
  • It is usually not associated with any symptoms but a minority of people develop other conditions caused by their unstable joints; in such cases, it is known as "'joints hypermobility syndrome "'( "'JHS "').
  • At age 6, Beth's symptoms-- elastic skin, widened scars, easy bruising, anal prolapse, joint hypermobility, lax muscles and little fatty cysts or " spheroids " on her forearms and shins-- indicated the so-called classical type of the syndrome.