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Thiamine deficiency is a medical condition of low levels of thiamine (vitamin B 1). [1] A severe and chronic form is known as beriberi. [1] [7] The name beriberi was possibly borrowed in the 18th century from the Sinhalese phrase බැරි බැරි (bæri bæri, “I cannot, I cannot”), owing to the weakness caused by the condition.
The grotesque body is a concept, or literary trope, put forward by Russian literary critic Mikhail Bakhtin in his study of François Rabelais' work. The essential principle of grotesque realism is degradation, the lowering of all that is abstract, spiritual, noble, and ideal to the material level.
Weakness of the bulbar muscles (muscles of the mouth and throat) is occasionally encountered. [4] Weakness of the eye muscles is uncommon. Some may have double vision , drooping of the eyelids and difficulty swallowing , [ 4 ] but generally only together with leg weakness; this too distinguishes LEMS from myasthenia gravis, in which eye signs ...
Common symptoms present in the different types of leprosy include a runny nose; dry scalp; eye problems; skin lesions; muscle weakness; reddish skin; smooth, shiny, diffuse thickening of facial skin, ear, and hand; loss of sensation in fingers and toes; thickening of peripheral nerves; a flat nose from the destruction of nasal cartilages; and changes in phonation and other aspects of speech ...
Ghost sickness is a culture-bound syndrome among some indigenous peoples in North America and Polynesian peoples in which people are preoccupied with the deceased or consumed by pathological grief.
Weakness in the hip extensor muscles; Gastrocnemius muscle weakness (in standing position) Upper motor neuron lesion (for example, hemiplegia as the result of a cerebrovascular accident) Lower motor neuron lesion (for example, in post-polio syndrome) Deficit in joint proprioception; Lower limb length discrepancy; Congenital genu recurvatum ...
Spinal and bulbar muscular atrophy (SBMA), popularly known as Kennedy's disease, is a rare, adult-onset, X-linked recessive lower motor neuron disease caused by trinucleotide CAG repeat expansions in exon 1 of the androgen receptor (AR) gene, which results in both loss of AR function and toxic gain of function.