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  2. Marsili syndrome - Wikipedia

    en.wikipedia.org/wiki/Marsili_syndrome

    Marsili syndrome is an extremely rare genetic disorder which is characterized by symptoms similar to those reported on individuals with congenital insensitivity to pain with anhidrosis. It can be fatal if it goes unnoticed/undiagnosed.

  3. Hypohidrosis - Wikipedia

    en.wikipedia.org/wiki/Hypohidrosis

    The treatment options for hypohidrosis and anhidrosis are largely limited to preventing overheating, and attempting to resolve or prevent further deterioration of any known underlying causes. Those with hypohidrosis should avoid drugs that can aggravate the condition (see "Medications", under § Causes ).

  4. Congenital insensitivity to pain with anhidrosis - Wikipedia

    en.wikipedia.org/wiki/Congenital_insensitivity...

    Congenital insensitivity to pain with anhidrosis (CIPA) is a rare autosomal recessive disorder of the nervous system which prevents the feeling of pain or temperature and prevents a person from sweating. Cognitive disorders are commonly coincidental.

  5. Acquired idiopathic generalized anhidrosis - Wikipedia

    en.wikipedia.org/wiki/Acquired_idiopathic...

    The diagnostic criteria for acquired idiopathic generalized anhidrosis is as follows: [6] Despite the widespread distribution of idiopathic anhidrosis or hypohidrosis lesions in a non-segmental spinal pattern, no additional neurological or autonomic symptoms are noted. [6] At least 25% of the body is affected by anhidrotic or hypohidrotic regions.

  6. Hereditary sensory and autonomic neuropathy - Wikipedia

    en.wikipedia.org/wiki/Hereditary_sensory_and...

    The signs and symptoms of hereditary sensory neuropathy type 1 typically appear during a person's teens or twenties. While the features of this disorder tend to worsen over time, affected individuals have a normal life expectancy if signs and symptoms are properly treated. Type 1 is the most common form among the 5 types of HSAN.

  7. Idiopathic pure sudomotor failure - Wikipedia

    en.wikipedia.org/wiki/Idiopathic_pure_sudomotor...

    Idiopathic pure sudomotor failure (IPSF) is the most common cause of a rare disorder known as acquired idiopathic generalized anhidrosis (AIGA), a clinical syndrome characterized by generalized decrease or absence of sweating without other autonomic and somatic nervous dysfunctions and without persistent organic cutaneous lesions.

  8. Sleep apnea: causes, symptoms, treatments, and how it ... - AOL

    www.aol.com/lifestyle/sleep-apnea-causes...

    Untreated sleep apnea can lead to a host of symptoms over the short and long term. Short-term issues associated with the condition are fragmented sleep, difficulty concentrating, irritability or ...

  9. Hypohidrotic ectodermal dysplasia with immune deficiency

    en.wikipedia.org/wiki/Hypohidrotic_ectodermal...

    Little to no ability to sweat (hypo/anhidrosis) Frontal bossing (prominence of the forehead) Wrinkling under the eyes; Periorbital hyperpigmentation; These symptoms are accompanied by an immunodeficiency that affects the entire body and impairs the body's antibody response (especially that to polysaccharides).