Hyporeflexia

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Carlos A Lopez, M.D. [2]

Causes

Life Threatening Causes

Life-threatening causes include conditions which may result in death or permanent disability within 24 hours if left untreated.

Causes by Organ System

Cardiovascular	Stroke
Chemical / poisoning	Aftershave, barium sulfate, selenious acid, cone shell poisoning, erythrokeratodermia ataxia, eucalyptus oil poisoning, licorice, herbal agent overdose cleistanthus collinus, opioid intoxication, oriental hornet poisoning , snakebites, sea snake poisoning , white chameleon poisoning
Dermatologic	Vitamin E deficiency
Drug Side Effect	All-trans retinoic acid, cevimeline, clonidine, fluphenazine, imidazoline, lamotrigine, vincristine,lorazepam, nelarabine, oxazepam, oxcarbazepine, perphenazine, phenothiazine, prochlorperazine, saquinavir, thioridazine, tiagabine, trifluoperazine, venlafaxine, vigabatrin, zaleplon
Ear Nose Throat	ARTS syndrome
Endocrine	Hypokalemic thyrotoxic periodic paralysis
Environmental	No underlying causes
Gastroenterologic	Chylomicron retention disease
Genetic	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
Hematologic	Tang Hsi Ryu syndrome
Iatrogenic	No underlying causes
Infectious Disease	Lyme disease, quaternary syphilis, tabes dorsalis
Musculoskeletal / Ortho	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, hypokalemic thyrotoxic 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, transverse myelitis, Treft-sanborn-carey syndrome, Zellweger syndrome
Neurologic	Acute weakness in the emergency department, Arts syndrome , Brown-sequard (hemi-cord) syndrome, Bulimia nervosa, Camfak syndrome , Cauda equina syndrome, Central cord syndromes, Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss , Cerebellar syndrome, Cerebro-oculo-facio-skeletal syndrome , Charcot-marie-tooth disease, type 2 , Charcot-marie-tooth disease, type 2i , Charcot-marie-tooth disease, type 2l , Charcot-marie-tooth disease, x-linked , Choreoacanthocytosis amyotrophic , Coloboma chorioretinal cerebellar vermis aplasia , Conus medullaris syndrome , Decreased folate , Dorsal (posterior) cord syndrome, Down's syndrome-like hypotonia , Familial isolated deficiency of vitamin e , Friedreich ataxia, Gerstmann-sträussler-scheinker syndrome, Hypertrophic neuropathy of dejerine-sottas , Infantile axonal neuropathy , Krabbe disease, atypical, due to saposin a deficiency , Marinesco-sjogren syndrome , Miller fisher syndrome, Muscular dystrophy -- white matter spongiosis , Navajo neurohepatopathy , Nervous system injuries due to penetrating neck injury, Paramyotonia congenita , Peripheral nerve and muscle disease, Proximal spinal muscular atrophy , Pure motor syndrome, Quaternary syphilis, Rommen-mueller-sybert syndrome , Segmental syndrome, Spinal cord inflammation or compression, Spinocerebellar ataxia, Stroke, Transverse myelitis , Ventral (anterior) cord syndrome,
Nutritional / Metabolic
Obstetric/Gynecologic	No underlying causes
Oncologic
Ophthalmologic	No underlying causes
Overdose / Toxicity	No underlying causes
Psychiatric
Pulmonary
Renal / Electrolyte
Rheum / Immune / Allergy	multifocal motor neuropathy with conduction block
Sexual	No underlying causes
Trauma	No underlying causes
Urologic	No underlying causes
Miscellaneous

See also

• Areflexia, the absence of reflexes, often it is caused by spinal shock.
• Hyperreflexia, exaggerated reflexes.

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