Hyporeflexia: Difference between revisions
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| '''Genetic''' | | '''Genetic''' | ||
|bgcolor="Beige"| [[Jansen's metaphyseal chondrodysplasia]], [[Lambert-Eaton myasthenic syndrome]], [[leigh's disease]], [[lower motor neuron lesion]], [[marinesco-Sjogren syndrome]], [[NADH CoQ reductase deficiency]], [[McLeod phenotype]], [[mental retardation, x-linked, 94]], [[miller fisher syndrome]], [[mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes]], multifocal motor neuropathy with conduction block, navajo neurohepatopathy, [[infantile neuroaxonal dystrophy]], neuronal intranuclear hyaline inclusion disease, | |bgcolor="Beige"| [[Jansen's metaphyseal chondrodysplasia]], [[Lambert-Eaton myasthenic syndrome]], [[leigh's disease]], [[lower motor neuron lesion]], [[marinesco-Sjogren syndrome]], [[NADH CoQ reductase deficiency]], [[McLeod phenotype]], [[mental retardation, x-linked, 94]], [[miller fisher syndrome]], [[mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes]], multifocal motor neuropathy with conduction block, navajo neurohepatopathy, [[infantile neuroaxonal dystrophy]], neuronal intranuclear hyaline inclusion disease, distal hereditary motor type VII, [[non-ketotic hyperglycemia]], Pena-shokeir syndrome type 2, [[progressive external opthhalmoplegia, autosomal dominant, 1]], [[Roussy-levy syndrome]], [[Smith-Magenis syndrome]], Southwestern athabaskan genetic diseases, [[spastic tetraplegic -- cerebral palsy]], spinal bulbar motor neuropathy, [[spinal muscular atrophy]], [[spinocerebellar ataxia]] | ||
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| '''Musculoskeletal / Ortho''' | | '''Musculoskeletal / Ortho''' | ||
|bgcolor="Beige"| [[Adducted thumb syndrome recessive form]], | |bgcolor="Beige"| [[Adducted thumb syndrome recessive form]], [[arthrogryposis due to muscular dystrophy]], [[becker muscular dystrophy]], [[benign congenital hypotonia]], [[brown-Sequard syndrome]], [[bulimia nervosa]], [[CAMFAK syndrome]], [[cauda equina syndrome]], [[cerebro-Oculo-Facio-Skeletal syndrome]], [[charcot-Marie-Tooth disease, type 2]], [[cockayne syndrome]], [[complex 1 mitochondrial respiratory chain deficiency]], [[congenital myopathy]], [[conus medullaris syndrome]], distal hereditary motor type VII, [[Down's syndrome]], [[Duchenne muscular dystrophy]], [[Dykes-Markes-Harper syndrome]], emerinopathy, Erb-goldflam, [[Fazio Londe syndrome ]], [[Gerstmann-Straussler-Scheinker syndrome]], [[Guillain-Barré syndrome]], [[Holmes-Adie syndrome]], [[hyperkalemic periodic paralysis]], [[hypokalemic periodic paralysis]], [[Lambert-Eaton myasthenic syndrome]], [[lower motor neuron lesion]], [[muscular dystrophy]], [[multifocal muscular fibrosis]], nervous system injuries due to penetrating neck injury, [[Infantile neuroaxonal dystrophy]], neuronal intranuclear hyaline inclusion disease, [[paramyotonia congenita]], penetrating neck injuries, peripheral nerve and muscle disease, [[polymyositis]], progressive external opthhalmoplegia, rommen-mueller-sybert syndrome, scapuloperoneal amyotrophy, schwartz-jampel syndrome, [[Smith-Magenis syndrome]], [[spinal cord compression]], [[spinal muscular atrophy]], | ||
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[[Thoracic dysplasia -- hydrocephalus syndrome ]], | [[Thoracic dysplasia -- hydrocephalus syndrome ]], | ||
Revision as of 15:29, 15 November 2015
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Carlos A Lopez, M.D. [2]
Overview
Causes
Life Threatening Causes
Life-threatening causes include conditions which may result in death or permanent disability within 24 hours if left untreated.
Common Causes
Causes by Organ System
Causes in Alphabetical Order
References
References
See also
- Areflexia, the absence of reflexes, often it is caused by spinal shock.
- Hyperreflexia, exaggerated reflexes.