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Results 1 - 8 of 8 for Abnormal pyramidal sign
  1. Behcet Disease From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Behcet's Syndrome/Learn More ... Behcet's Syndrome ... Genetic and Rare Diseases Information Center ... From the National Institutes of Health ... Find symptoms and other ...
    https://rarediseases.info.nih.gov/diseases/848/behet-disease - External Health Links
  2. Fatty acid hydroxylase-associated neurodegeneration 
    Fatty acid hydroxylase-associated neurodegeneration (FAHN) is a progressive disorder of the nervous system (neurodegeneration) characterized by problems with ...
    https://medlineplus.gov/...-hydroxylase-associated-neurodegeneration - Genetics
  3. Spastic paraplegia type 3A 
    ... in the lower limbs, reduced bladder control, an abnormal curvature of the spine (scoliosis), loss of sensation in the feet (peripheral neuropathy), or high arches of the feet (pes cavus). The signs and symptoms of spastic paraplegia type 3A usually ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-3a - Genetics
  4. Silver syndrome 
    ... is a complex hereditary spastic paraplegia.The first sign of Silver syndrome is usually weakness in the muscles of the hands. These muscles waste away (amyotrophy), resulting in abnormal positioning of the thumbs and difficulty using the ...
    https://medlineplus.gov/genetics/condition/silver-syndrome - Genetics
  5. Hypomyelination with brainstem and spinal cord involvement and leg spasticity 
    ... Other neurological problems in affected individuals can include abnormal side-to-side ... column. ...
    https://medlineplus.gov/...pinal-cord-involvement-and-leg-spasticity - Genetics
  6. Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation 
    ... within the brainstem and spinal cord, especially the pyramidal tract and the dorsal column. In addition, most ... unclear how the gene mutations lead to the signs and symptoms of LBSL. Researchers do not understand ...
    https://medlineplus.gov/...al-cord-involvement-and-lactate-elevation - Genetics
  7. ATL1 gene 
    ... mutation is associated with hereditary sensory neuropathy and pyramidal tract features. Eur J Neurol. 2012 Jul;19( ...
    https://medlineplus.gov/genetics/gene/atl1 - Genetics
  8. C19orf12 gene 
    ... Alkuraya F. C19orf12 mutation leads to a pallido-pyramidal syndrome. Gene. 2014 Mar 10;537(2):352- ...
    https://medlineplus.gov/genetics/gene/c19orf12 - Genetics