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tuberous sclerosis |
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sclerosis /scle·ro·sis/ (-ro´sis) an induration or hardening, especially from inflammation and in diseases of the interstitial substance; applied chiefly to such hardening of the nervous system or to hardening of the blood vessels. amyotrophic lateral sclerosis Lou Gehrig disease: progressive degeneration of the neurons that give rise to the corticospinal tract and of the motor cells of the brain stem and spinal cord, resulting in a deficit of upper and lower motor neurons; it usually has a fatal outcome within 2 to 3 years. arterial sclerosis arteriosclerosis. arteriolar sclerosis arteriolosclerosis. diffuse cerebral sclerosis the infantile form of metachromatic leukodystrophy. disseminated sclerosis multiple s. familial centrolobar sclerosis Pelizaeus-Merzbacher disease. glomerular sclerosis glomerulosclerosis. hippocampal sclerosis loss of neurons in the region of the hippocampus, with gliosis; sometimes seen in epilepsy. lateral sclerosis degeneration of the lateral columns of the spinal cord, leading to spastic paraplegia. See amyotrophic lateral sclerosis and primary lateral sclerosis Mönckeberg's sclerosis see under arteriosclerosis. multiple sclerosis (MS) demyelination occurring in patches throughout the white matter of the central nervous system, sometimes extending into the gray matter; symptoms of lesions of the white matter are weakness, incoordination, paresthesias, speech disturbances, and visual complaints. primary lateral sclerosis a form of motor neuron disease in which the degenerative process is limited to the corticospinal pathways. progressive systemic sclerosis systemic scleroderma. tuberous sclerosis an autosomal dominant disease characterized by hamartomas of the brain (tubers), retina, and viscera; mental retardation; seizures; and adenoma sebaceum.
Tuberous sclerosis A genetic disease that causes skin problems, seizures, and mental retardation. It may be confused with autism. Mentioned in: Autism tuberous sclerosis, a familial, neurocutaneous disease characterized by epilepsy, mental deterioration, adenoma sebaceum, nodules and sclerotic patches on the cerebral cortex, retinal tumors, depigmented leaf-shaped macules on the skin, tumors of the heart or kidneys, and cerebral calcifications. There is no effective treatment. Also called Bourneville's disease, epiloia. See also adenoma sebaceum. tuberous sclerosis Internal medicine An AD neurocutaneous syndrome characterized by skin lesions, variable mental retardation and seizures; TS is named after the typical brain lesion–a tuber. See Neurocutaneous disorder.
Tuberous sclerosis –gomez criteria
Primary† Secondary‡
Facial angiofibroma 1º relative with TS
Fibrous plaque on forehead Hypomelanic macules
Ungual fibroma Shagreen patch
Cortical tuber Infantile spasms
Multiple retinal hamartomas Single retinal hamartoma
Subependymal hamartoma Cardiac rhabdomyoma
Bilateral renal angiomyolipomas or cysts
†One required for diagnosis‡Two required for diagnosis
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