ಎರಡೂ ಕಾಲುಗಳಲ್ಲಿ ಸ್ವಲ್ಪ ಪಾರ್ಶ್ವವಾಯು ಅಥವಾ ದೌರ್ಬಲ್ಯ,

paraparesis's Usage Examples:

Fibromuscular dysplasia FMS Fibromyalgia syndrome FSP Familial spastic paraparesis FTD Frontotemporal dementia FUO Fever of unknown origin FVS Fetal valproate.

in VPS37A protein has been shown to cause complex hereditary spastic paraparesis (cHSP).

HSP is also known as hereditary spastic paraparesis, familial spastic paraplegia, French.

GBA2 genes are rare causes of complicated forms of hereditary spastic paraparesis" (PDF).

HSP is also known as hereditary spastic paraparesis, familial spastic paraplegia, French settlement disease, Strumpell disease, or Strumpell-Lorrain.

type Spastic dysphonia Spastic p Spastic paraparesis deafness Spastic paraparesis, infantile Spastic paraparesis Spastic paraplegia epilepsy mental retardation.

symptoms, including: Konzo Tropical spastic paraparesis (TSP) Tropical ataxic neuropathy (TAN) TAN is poorly understood, and some researchers subdivide.

demyelinating disease called HTLV-1 associated myelopathy/tropical spastic paraparesis (HAM/TSP).

suffered childhood poliomyelitis with residual left lower-extremity paraparesis, complicated by severe talipes.

clinical severity, ranging from adrenal insufficiency to progressive paraparesis in early adulthood (this form of the disease is typically known as.

upper motor neuron signs in the lower limbs, presenting as a spastic paraparesis.

neuron disease known as HTLV-1 associated myelopathy/tropical spastic paraparesis (HAM/TSP), characterized by sensory and motor deficits, particularly.

HSP is also known as hereditary spastic paraparesis, familial spastic paraplegia, French settlement disease, Strumpell disease.