enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Tension myositis syndrome - Wikipedia

    en.wikipedia.org/wiki/Tension_myositis_syndrome

    Tension myositis syndrome (TMS), also known as tension myoneural syndrome or mindbody syndrome, is a name given by John E. Sarno to what he claimed was a condition of psychogenic musculoskeletal and nerve symptoms, most notably back pain.

  3. Pallister–Killian syndrome - Wikipedia

    en.wikipedia.org/wiki/Pallister–Killian_syndrome

    The Pallister–Killian syndrome (PKS), also termed tetrasomy 12p mosaicism or the Pallister mosaic aneuploidy syndrome, is an extremely rare and severe genetic disorder. PKS is due to the presence of an extra and abnormal chromosome termed a small supernumerary marker chromosome (sSMC). sSMCs contain copies of genetic material from parts of ...

  4. Congenital myasthenic syndrome - Wikipedia

    en.wikipedia.org/wiki/Congenital_myasthenic_syndrome

    Congenital myasthenic syndrome ( CMS) is an inherited neuromuscular disorder caused by defects of several types at the neuromuscular junction. The effects of the disease are similar to Lambert-Eaton Syndrome and myasthenia gravis, the difference being that CMS is not an autoimmune disorder. There are only 600 known family cases of this disorder ...

  5. Say Goodbye To Sciatica Pain By Stretching These Two Muscles

    www.aol.com/goodbye-sciatica-pain-stretching-two...

    Sciatica can vary from a mild ache to a sharp burning sensation, and some people may also experience numbness or tingling in the leg or foot, per the Mayo Clinic. If you struggle with sciatica ...

  6. Prader–Willi syndrome - Wikipedia

    en.wikipedia.org/wiki/Prader–Willi_syndrome

    Prader–Willi syndrome ( PWS) is a rare genetic disorder caused by a loss of function of specific genes on chromosome 15. [2] In newborns, symptoms include weak muscles, poor feeding, and slow development. [2] Beginning in childhood, those affected become constantly hungry, which often leads to obesity and type 2 diabetes. [2]

  7. Trisomy 18 - Wikipedia

    en.wikipedia.org/wiki/Trisomy_18

    1 per 5,000 births [3] Trisomy 18, also known as Edwards syndrome, is a genetic disorder caused by the presence of a third copy of all or part of chromosome 18. [3] Many parts of the body are affected. [3] Babies are often born small and have heart defects. [3] Other features include a small head, small jaw, clenched fists with overlapping ...

  8. Juvenile dermatomyositis - Wikipedia

    en.wikipedia.org/wiki/Juvenile_dermatomyositis

    Juvenile dermatomyositis ( JDM) is an idiopathic inflammatory myopathy (IMM) of presumed autoimmune dysfunction resulting in muscle weakness among other complications. It manifests itself in children; it is the pediatric counterpart of dermatomyositis. In JDM, the body's immune system attacks blood vessels throughout the body, causing ...

  9. What is trisomy 18? Why the fatal genetic disorder is in the ...

    www.aol.com/lifestyle/trisomy-18-why-fatal...

    The Cleveland Clinic breaks down the devastating statistics for children with trisomy 18 who survive past birth: 60% to 75% survive to their first week. 20% to 40% survive to their first month.