ⓘ Acquired idiopathic generalized anhidrosis

                                     

ⓘ Acquired idiopathic generalized anhidrosis

Acquired idiopathic generalized anhidrosis is characterized by generalized absence of sweating without other autonomic and neurologic dysfunction.

Aiga is divided into 3 subgroups: idiopathic pure sudomotor failure FVKN, sweat glands GFS failure, and sudomotor neuropathy, with each subgroup represents a Different pathogenesis.

                                     
  • Idiopathic pure sudomotor failure IPSF is the most common cause of a rare disorder known as acquired idiopathic generalized anhidrosis AIGA a clinical
  • relation to sporting activities. Sweat hypersensitivity Acquired anhidrosis and or hypohidrosis Idiopathic Opioid use Cholinesterase inhibitors This subtype
  • Generalized discoid lupus erythematosus Generalized morphea Interstitial granulomatous dermatitis Juvenile rheumatoid arthritis juvenile idiopathic arthritis
  • occlusion, which produces anhidrosis and heat retention. Occlusion miliaria is a skin condition that is accompanied by anhidrosis and increased heat - stress
  • crystallina L74.2 Miliaria profunda L74.3 Miliaria, unspecified L74.4 Anhidrosis L74.8 Other eccrine sweat disorders L74.9 Eccrine sweat disorder