What is spastic paraplegia type 11?
Spastic paraplegia type 11 is part of a group of genetic disorders known as hereditary spastic paraplegias.
Hereditary spastic paraplegia (HSP), also called familial spastic paraparesis (FSP), refers to a group of inherited disorders that are characterized by progressive weakness and spasticity (stiffness) of the legs.
Hereditary spastic paraplegia, autosomal dominant: A degenerative disorder of nerves with progressive spasticity of the legs. Abbreviated as AD-HSP.
Autosomal recessive complex spastic paraplegia
Orpha number
ORPHA100981 ...
spastic paraplegia
spstk pr plid noun paralysis of one side of the body after a stroke
spatula ...
spastic paraplegia type 3A - caused by mutations in the ATL1 gene More than 30 mutations in the ATL1 gene have been identified in people with spastic paraplegia type 3A.
Erb's spastic paraplegia. , Erb's syphilitic spastic paraplegia an uncommon form of meningovascular syphilis marked by progressive spasticity and weakness of the legs, paraplegia, muscular atrophy, paresthesia, increased knee and ankle reflexes, ...
Familial Spastic Paraplegia
FSP
HSP
Spastic Spinal Familial Paralysis
Strumpell's Familial Paraplegia
Strumpell-Lorrain Familial Spasmodic Paraplegia
Strumpell Disease
Strumpell-Lorraine Syndrome ...
Hereditary spastic paraplegia (HSP), also called familial spastic paraparesis, is characterized by progressive spasticity in the lower extremities that can become severe and incapacitating.
Hereditary spastic paraplegia (HSP): Hereditary spastic paraplegia or HSP is a group of genetic disorders that affects the spinal cord and results in weakness and stiffness of the legs.
Autosomal recessive spastic paraplegia, type 11:
Avascular necrosis of femoral head, ...
X linked Recessive Hereditary Spastic Paraplegia
X Radiation
X Radiations
X Ray Absorptiometry, Dual Energy
X Ray Computed Tomography Scanner
X Ray Computed Tomography Scanners
X Ray Crystallographies
X Ray Crystallography
X Ray Department ...
Autosomal dominant hereditary spastic paraplegia, Directory, Dysfunction, Multiple Peroxisomal, FMRFamide, Genes, Lac, Gonadotropin Resistant Ovary Syndrome, Heterologous Antigens, Idioventricular Rhythms, Accelerated, Infection, Phasmidia, ...
Familial Spastic Paraparesis see Familial Spastic Paraplegia
Familial Spastic Paraplegia
Fanconi Anaemia
Fanconi Anemia see Fanconi Anaemia
Fanconi's Anaemia see Fanconi Anaemia
FAS see Fetal Alcohol Spectrum disorder
Fatty Acid Oxidation disorders ...
Also known as the Sjogren-Larsson syndrome, this is a genetic (inherited) disease usually characterized by a triad of clinical findings consisting of ichthyosis (thickened fish-like skin), spastic paraplegia (spasticity of the legs) and mental ...
Genetic disorder (hereditary spastic paraplegia)
Congenital (present at birth)
Infection
Autoimmune diseases
Tumor (either within the spinal cord or compressing the spinal cord)
Syrinx (a spinal chord disorder) ...
Spastic diplegia
Pernicious anemia
Spastic paraplegia
This short section requires expansion.
Familial Spastic Paraplegia
Familial Startle Disease
Familial Testotoxicosis
Families Anonymous - Support Group
Families Anonymous - Support Group
Families Anonymous - Alcohol Abuse - Support Group ...
Fahr syndrome thus involves abnormalities of the neurologic system (cerebral calcification, dementia, spastic paraplegia, athetosis), skull (microcephaly, i.e. an abnormally small head), eyes (glaucoma, optic nerve atrophy, retinitis pigmentosa), ...
Associated features often include underdevelopment (hypoplasia) and wasting (atrophy) of muscle tissue; weakness and stiffness of the legs (spastic paraplegia) with exaggerated reflexes (hyperreflexia); relatively slow, involuntary, purposeless, ...
condition in which there is constant, slow, involuntary, writhing movement of the fingers/hands or feet/toes. It typically occurs due to brain injury or disease (or medications that can effect the brain). An example is congenital spastic paraplegia ...
 See also: Paraplegia, Plegia, Symptom, Cancer, Stroke
  
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