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98 Possible Causes for Hyporeflexia in the Lower Limbs, Muscular Atrophy

  • Guillain-Barré Syndrome

    RESULTS: All six patients had different degrees of muscular atrophy at nadir and in two, respiratory muscles were involved.[ncbi.nlm.nih.gov] Physical examination confirmed lower left facial palsy and paresthesia of his extremities with hyporeflexia of his lower limbs and sensory loss of all four extremities.[ncbi.nlm.nih.gov] The peroneal muscular atrophy syndrome 8. The ataxic neuropathies 9. Sensory neuropathies 10. Neuropathies in metabolic and degenerative disorders 11.[scinapse.io]

  • Poliomyelitis

    We report the case of PPS in a patient, 40 years, that thirty-five years after had had paralytic poliomyelitis, developed new symptoms of fatigue, muscular atrophy, dyspnea[ncbi.nlm.nih.gov] Some of these patients develop post-poliomyelitis muscular atrophy (PPMA) which is characterized by a slowly progressive muscle weakness.[ncbi.nlm.nih.gov] Some of these patients develop slowly progressive muscle weakness known as post-poliomyelitis muscular atrophy (PPMA).[ncbi.nlm.nih.gov]

  • Déjerine-Sottas Disease

    He is currently involved in multiple clinical trials of novel genetic interventions for the treatment of spinal muscular atrophy and Duchenne muscular dystrophy. Dr. H.[books.google.com] A 9-year-old boy presented progressive slight motor deficit in the lower limbs, particularly in the feet, and generalized hyporeflexia.[ncbi.nlm.nih.gov] CASE REPORT: A 9-year-old boy presented progressive slight motor deficit in the lower limbs, particularly in the feet, and generalized hyporeflexia.[anestesiarianimazione.com]

  • Autosomal Dominant Spastic Paraplegia Type 31

    He is currently involved in multiple clinical trials of novel genetic interventions for the treatment of spinal muscular atrophy and Duchenne muscular dystrophy. Dr. H.[books.google.ro] limb amyotrophy Proximal muscle weakness Corpus callosum atrophy Spastic dysarthria Hyporeflexia of lower limbs Titubation Impaired distal vibration sensation Temporal optic[mendelian.co] The overall clinical picture consists of a classical distal muscular atrophy syndrome in the legs without clinical sensory loss.[genecards.org]

  • Autosomal Dominant Spastic Ataxia Type 1

    Distal sensory deficits with lack of sensory nerve action potentials are also present in the lower limbs.[disorders.eyes.arizona.edu] He is currently involved in multiple clinical trials of novel genetic interventions for the treatment of spinal muscular atrophy and Duchenne muscular dystrophy. Dr. H.[books.google.com] . : Peroneal muscular atrophy (MPA) and related disorders. II. Histological finding in sural nerves . Brain 100:67–85, 1977.[link.springer.com]

  • Autosomal Dominant Spastic Paraplegia Type 17

    SPG17 is a motor neuron disease overlapping with distal spinal muscular atrophy type 5.[mybiosource.com] He presented with progressive spastic paraplegia, hypereflexia in the upper limbs with hyporeflexia in the lower limbs. There was dysdiadochokinesis.[nature.com] Disease description A disorder characterized by distal muscular atrophy mainly affecting the upper extremities, in contrast to other distal motor neuronopathies.[uniprot.org]

  • Zebra Body Myopathy

    Neck muscle weakness Lower limb muscle weakness Generalized hypotonia Difficulty climbing stairs Motor delay Rare Symptoms - Less than 30% cases Difficulty walking Hyperlordosis[mendelian.co] He is currently involved in multiple clinical trials of novel genetic interventions for the treatment of spinal muscular atrophy and Duchenne muscular dystrophy.[books.google.com] atrophy Proximal spinal muscular atrophy type 1 Proximal spinal muscular atrophy type 2 Proximal spinal muscular atrophy type 3 Proximal spinal muscular atrophy type 4 Rare[se-atlas.de]

  • Myofibrillar Myopathy Type 4

    atrophies – a single centre study of 43 pediatric patients Lindsay Wallace The DUX4 promoter mouse: the next generation[worldmusclesociety.org] Diagnosed with spinal muscular atrophy (SMA) when he was 1 year old, Och fondly remembers the time he spent at MDA Summer Camp during his childhood.[quest.mda.org] The following genes are required for Invitae carrier screening and will be added to your order, CFTR (cystic fibrosis), SMN1 (spinal muscular atrophy), FMR1 (fragile X syndrome[invitae.com]

  • Congenital Muscular Dystrophy due to LMNA Mutation

    Neurological examination revealed moderate amyotrophy and mild proximal weakness in the lower limbs, hyporeflexia, and syndactyly of the fourth and fifth fingers of the right[jnnp.bmj.com] He is currently involved in multiple clinical trials of novel genetic interventions for the treatment of spinal muscular atrophy and Duchenne muscular dystrophy.[books.google.com] ATROPHIES & MOTOR NEURON DISEASES Spinal muscular atrophy, type I-IV (SMN1) Spinal muscular atrophy, autosomal dominant, proximal, adult-onset (VAPB) Spinal muscular atrophy[meduniwien.ac.at]

  • CAMFAK Syndrome

    […] distal spinal muscular atrophy ) 脊肌萎缩症伴有小脑发育不全 ( 英语 : Spinal muscular atrophy with pontocerebellar hypoplasia ) 脊肌萎缩症伴有较低极限优势 ( 英语 : Spinal muscular atrophy with lower extremity[knowpia.cn] […] growth retardation Severe intrauterine growth retardation Tics Hyporeflexia Constipation Respiratory failure Hyperhidrosis Distal muscle weakness Lower limb muscle weakness[mendelian.co] atrophy type 1 ) 二型X染色体相关的脊髓性肌肉萎缩症 ( 英语 : X-linked spinal muscular atrophy type 2 ) 一型家族远端型脊肌萎缩症 ( 英语 : Distal spinal muscular atrophy type 1 ) 先天性远端型脊肌萎缩症 ( 英语 : Congenital[knowpia.cn]

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