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19 Possible Causes for Hypesthesia, Onset at Age 5-10 Years, Restless Legs Syndrome

  • Diabetes Mellitus Type 2

    Epidemiology Type 1 : 5% of all patients with diabetes Childhood onset ; : typically 20 years but can occur at any age; peaks at age 4–6 years and 10–14 years Highest prevalence[amboss.com]

  • Primary Progressive Multiple Sclerosis

    […] and especially early age at onset, are associated with a better course. [13] [114] The average life expectancy is 30 years from the start of the disease, which is 5 to 10[en.wikipedia.org] Long term [1] Causes Unknown [3] Diagnostic method Based on symptoms and medical tests [4] Treatment Medications, physical therapy [1] Prognosis 510 year shorter life expectancy[en.wikipedia.org] Specialty Neurology Symptoms Double vision, blindness in one eye, muscle weakness, trouble with sensation, trouble with coordination [1] Usual onset Age 20–50 [2] Duration[en.wikipedia.org]

  • Multiple Sclerosis

    syndrome (RLS).[ncbi.nlm.nih.gov] Table 1 Patient demographics Female 319 (64%) Male 178 (36%) Age 5 (1%) 21–30 86 (17%) 31–40 151 (30%) 41–50 143 (29%) 60 112 (23%) Onset 143 (29%) 5–10 years ago 177 (36%[dx.doi.org] […] and especially early age at onset, are associated with a better course.[13][115] The average life expectancy is 30 years from the start of the disease, which is 5 to 10 years[en.wikipedia.org]

  • Diabetic Neuropathy

    Abstract We investigated three diabetic patients whose neuropathy was characterized by pain, hypesthesia, and autonomic dysfunction, with preservation of epicritic sensation[ncbi.nlm.nih.gov] […] of DM Symptomatic evidence 5 years: 4% to 10% 25 years: 13% to 15% Mean time after DM onset: 8 years Increased Frequency: Women; Increased Age Objective evidence (Clinical[neuromuscular.wustl.edu] NEUROPATHIES: SYMMETRIC Chronic Distal: Sensory Autonomic Epidemiology: Risk factors & associations Most common type of diabetic neuropathy Temporal risk of neuropathy after onset[neuromuscular.wustl.edu]

  • Amyotrophic Lateral Sclerosis

    Restless Legs Syndrome Study Group.[doi.org] The male to female ratio is 2:1. [ 3 ] About 5-10% of cases are inherited. [ 5 ] The mean age of onset is 43-52 years in familial and 58-63 years in sporadic cases of ALS.[patient.info] (m/f: 41/15; mean age: 57.9   12.2 years), 15 patients with bulbar onset (m/f: 10/5; age: 59.0   8.4 years) and three patients with respiratory onset (m/f: 2/1; age: 62.0[onlinelibrary.wiley.com]

  • Tics

    Restless leg syndrome (RLS) has been reported in up to 10% of patients with TS.[childneurologyfoundation.org] In most children, the severity peaks at nine to 11 years of age. About 5 to 10 percent of patients have an intensifying course with little or no improvement.[aafp.org] Onset typically occurs before seven years of age and the disorder is usually recognized two to three years after onset.[aafp.org]

  • Young Adult-Onset Distal Hereditary Motor Neuropathy

    Hypesthesia and decreased vibratory sense are present in about half of cases.[clinicalgate.com] Symptomatic therapy of neuropathic pain, joint/bone pain, paresthesias, cramps, fatigue, and restless leg syndrome is done as for other neuropathies. 35.1.1.8 Prognosis Genetic[neupsykey.com] The male to female ratio is 2:1. [ 3 ] About 5-10% of cases are inherited. [ 5 ] The mean age of onset is 43-52 years in familial and 58-63 years in sporadic cases of ALS.[patient.info]

  • Paraparesis

    Hypesthesia and hypalgesia below the left L1 dermatome and anesthesia and analgesia below the right Th8 dermatome were observed.[nature.com] leg syndrome.[doctorshealthpress.com] Clinical description Pancreatoblastoma most often presents in children under the age of 10 (mean of 5 years).[orpha.net]

  • Charcot-Marie-Tooth Disease

    Postoperatively, in both patients, the back pain resolved immediately, there was a significant improvement of both the paresis of the legs and the hypesthesia, and there was[ncbi.nlm.nih.gov] Onset is usually by the age of 10 years with: Muscle weakness and wasting starting from the intrinsic muscles of the feet, and gradually affecting the lower leg and lower[patient.info] Ondo W, Jankovic J (1996) Restless legs syndrome: clinicoetiologic correlates. Neurology 47:1435–1441 PubMed Google Scholar 30.[doi.org]

  • Autosomal Recessive Lower Motor Neuron Disease with Childhood Onset

    . Fasciculation;myalgia, and hypesthesia No Definite cause has been determined 48.  Slowly progressive, asymmetrical muscle weaknessand atrophy Multifocal conduction block[slideshare.net] The onset can occur at any age in adult life, but most patients are more over 50 years of age.[neuroweb.us] Reflexes, vibration, and position sense are imparired -Main autosomal dominant ataxias -Commonly present with neuropathy, pyramidal signs, ataxia, and restless leg syndrome[quizlet.com]

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