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63 Possible Causes for Hyporeflexia (Later), Muscle Hypotonia

Did you mean: Hyporeflexia (Later, Muscle Hypotonia

  • Motor Neuron Disease

    , hyperreflexia and atrophy in later stages of disease, but fasciculations are absent.[symptoma.com] Loss of lower motor neurons causes denervation atrophy of muscle, manifested by severe hypotonia, weakness, and inability to breathe.[neuropathology-web.org] Symptoms may include hypotonia (severely reduced muscle tone), diminished limb movements, lack of tendon reflexes, fasciculations, tremors, swallowing and feeding difficulties[web.archive.org]

  • Myelopathy

    Nerve root compression commonly causes early radicular pain; later, there may be weakness, hyporeflexia, and muscle atrophy.[merckmanuals.com]

  • Autosomal Recessive Spinocerebellar Ataxia Type 17

    SCA2 differs clinically from other types of SCAs because of the slow saccade and hyporeflexia [ 22 ].[e-jmd.org] Hypotonia is a decrease in the normal resistance offered by muscles to passive manipulation When an affected limb is shaken flapping movements of the hands appear of wider[slideshare.net] Common features of XLAG include muscle spasticity, hypotonia, epilepsy, abnormal genitalia, developmental delay, and severe intellectual disability.[chginc.org]

  • Autosomal Recessive Spinocerebellar Ataxia 18

    SCA2 differs clinically from other types of SCAs because of the slow saccade and hyporeflexia [ 22 ].[e-jmd.org] Hypotonia is a decrease in the normal resistance offered by muscles to passive manipulation When an affected limb is shaken flapping movements of the hands appear of wider[slideshare.net] SCA2 may present parkinsonism or amyotrophic lateral sclerosis [ 23, 24 ], and cognitive impairment has also been reported for this subtype.[e-jmd.org]

  • Autosomal Recessive Spinocerebellar Ataxia

    SCA2 differs clinically from other types of SCAs because of the slow saccade and hyporeflexia [ 22 ].[e-jmd.org] SCA2 may present parkinsonism or amyotrophic lateral sclerosis [ 23, 24 ], and cognitive impairment has also been reported for this subtype.[e-jmd.org]

  • Familial Dysautonomia

    Esterly, et al46 reported on a patient with Pupillotonie, hyporeflexia and segmental hypohodrosis.[healio.com] The appearance of the tongue together with severe muscle hypotonia, absent or very sluggish tendon reflexes and swallowing difficulties in an infant born to one or both parents[rarediseasesjournal.com] Problems related to this disorder first appear in infants who show poor muscle tone (hypotonia), feeding difficulties, poor growth, lack of tears, frequent lung infections[jpost.com]

  • Vitamin B12 Deficiency

    In early stages, decreased position and vibratory sensation in the extremities is accompanied by mild to moderate weakness and hyporeflexia.[merckmanuals.com] hypotonia and somnolence.[ncbi.nlm.nih.gov] The child was exclusively breastfed until the fifth month of life, when he was hospitalised because of poor weight gain, feeding difficulties, severe pallor, muscle hypotonia[doi.org]

  • Ataxic Cerebral Palsy

    Adrenoleukodystrophy begins later in childhood, but other leukodystrophies begin earlier and may be mistaken for CP at first.[merckmanuals.com] Apart from affecting the actions of all the limbs, this condition also leads to hypotonia (a poor muscle tone).[speechtherapy.ygoy.com] For example: * With spasticity * With proximal hypertension * With athetosis * Expressed only in distal form Ataxia characteristic features * Low muscle tone - hypotonia *[questia.com]

  • Progressive Muscular Atrophy

    Babinski's sign positive) Flexor ( normal; Babinski's sign negative) Extraneous muscle activity No fasciculations/fibrillations Fasciculations and fibrillations amyotrophic lateral[medical-dictionary.thefreedictionary.com] Peripheral hypotonia that may affect any place between the spinal cord and muscle.[news-medical.net] Ocular and facial muscles and cerebral function are preserved. There may be deformities of limbs/joints at birth from in utero hypotonia.[patient.info]

  • Glycogen Storage Disease due to Phosphoglycerate Mutase Deficiency

    Muscle atrophy appears early and is accompanied by hyporeflexia.[euroformhealthcare.biz] hypotonia and death, usually before age 2, from cardiorespiratory failure Pompe’s Disease infantile Prgssve skltl muscle hypotonia w/o wasting, swallowing/breathing difficulty[quia.com] hypotonia, hypercholesterolemia Treatment: Nonspecific Type VIII/IXa: X-linked phosphorylase kinase PHKA2 (Xp22)* Type IXb Liver and muscle phosphorylase kinase PHKB (16q12[msdmanuals.com]

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