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139 Possible Causes for Slowly Progressive Spastic Paraplegia

  • Autosomal Recessive Spastic Paraplegia Type 46

    OMIM : 57 Autosomal recessive spastic paraplegia-46 (SPG46) is a neurodegenerative disorder characterized by onset in childhood of slowly progressive spastic paraplegia and[malacards.org] […] of slowly progressive spastic paraplegia of the lower extremities with bladder dysfunction and pes cavus or a complex presentation with additional manifestations including[rarediseases.info.nih.gov] 7; SPG7 Alt IDs: OMIM:607259, ICD10CM:G11.4, ORDO:99013 Definition: A hereditary spastic paraplegia that is characterized by slowly progressive onset, usually between 18-[informatics.jax.org]

  • Autosomal Dominant Spastic Paraplegia Type 42

    […] by slowly progressive spastic paraplegia of lower extremities with an age of onset ranging from childhood to adulthood and patients presenting with spastic gait, increased[orpha.net] paraplegia type 4; SPG4 Alt IDs: OMIM:182601, ICD10CM:G11.4, ORDO:100985 Definition: A hereditary spastic paraplegia that is characterized by slowly progressive muscle weakness[informatics.jax.org] Non-syndromic spastic paraplegias are characterized by slowly progressive spasticity and weakness of the lower extremity, often associated with hypertonic urinary disturbances[blueprintgenetics.com]

  • Autosomal Recessive Spastic Paraplegia Type 32

    Autosomal recessive spastic paraplegia type 32 (SPG32) is a rare, complex type of hereditary spastic paraplegia characterized by a slowly progressive spastic paraplegia (with[monarchinitiative.org] slowly progressive spastic paraplegia (with walking difficulties appearing at onset at 6-7 years of age) associated with mild intellectual disability.[rarediseases.info.nih.gov] Get Update Overview SPG30 is an autosomal recessive form of slowly progressive spastic paraplegia characterized by onset in the first or second decades of unsteady spastic[diseaseinfosearch.org]

  • Autosomal Dominant Spastic Paraplegia Type 41

    […] by onset in adolescence or early adulthood of slowly progressive spastic paraplegia, proximal muscle weakness of the lower extremities and small hand muscles, hyperreflexia[orpha.net] paraplegia type 4; SPG4 Alt IDs: OMIM:182601, ICD10CM:G11.4, ORDO:100985 Definition: A hereditary spastic paraplegia that is characterized by slowly progressive muscle weakness[informatics.jax.org] 1 Autosomal dominant pure spastic paraplegia (ADPSP) is clinically characterised by slowly progressive spasticity and weakness of the legs, hyperreflexia, and Babinski’s sign[jnnp.bmj.com]

  • Autosomal Recessive Spastic Paraplegia Type 63

    His intellect showed further deterioration at 15 years and he developed a slowly progressive spastic paraplegia at 17 years.[jnnp.bmj.com] 7; SPG7 Alt IDs: OMIM:607259, ICD10CM:G11.4, ORDO:99013 Definition: A hereditary spastic paraplegia that is characterized by slowly progressive onset, usually between 18-[informatics.jax.org] Family B Case IV-2B This 32 year old man developed a slowly progressive spastic paraplegia at 14 years and was confined to a wheelchair at 21 years.[jnnp.bmj.com]

  • Fitzsimmons-Guilbert Syndrome

    […] by a slowly progressive spastic paraplegia, skeletal anomalies of the hands and feet with brachydactyly type E, cone-shaped epiphyses, abnormal metaphyseal – phalangeal pattern[en.wikipedia.org] Abstract Fitzsimmons syndrome is an infrequently described entity comprising slowly progressive spastic paraplegia, brachydactyly, and cone-shaped epiphyses, dysarthria, and[ncbi.nlm.nih.gov] Fitzsimmons–Guilbert syndrome : Fitzsimmons–Guilbert syndrome is an extremely rare genetic disease characterized by a slowly progressive spastic paraplegia, skeletal anomalies[whatisthemeaningofname.com]

  • Fitzsimmons-McLachlan-Gilbert Syndrome

    […] by a slowly progressive spastic paraplegia, skeletal anomalies of the hands and feet with brachydactyly type E, cone-shaped epiphyses, abnormal metaphyseal – phalangeal pattern[en.wikipedia.org] Clinically, patients present with slowly progressive distal limb weakness and lower extremity spasticity.[reference.md] You can help by adding to it. ( July 2017 ) History [ edit ] Fitzsimmons and Guilbert first described male uniovular twins, aged 20 years, who had had slowly progressive spastic[en.wikipedia.org]

  • Paraplegia

    spastic paraplegia characterized by late childhood- to early adulthood-onset of slowly progressive spastic paraplegia with spastic gait and lower limb hyperreflexia, brisk[orpha.net] Clinically, patients present with slowly progressive distal limb weakness and lower extremity spasticity.[icd9data.com] Non-syndromic spastic paraplegias are characterized by slowly progressive spasticity and weakness of the lower extremity, often associated with hypertonic urinary disturbances[blueprintgenetics.com]

  • Hereditary Spastic Paraplegia

    Clinically, patients present with slowly progressive distal limb weakness and lower extremity spasticity.[icd9data.com] The diagnostic criteria of autosomal recessive hereditary spastic paraplegia with hypoplastic corpus callosum are inheritance consistent with autosomal recessive trait, slowly[ncbi.nlm.nih.gov] Hereditary spastic paraplegia with thin corpus callosum (HSP-TCC) is a frequent subtype of complicated HSP clinically characterized by a slowly progressive spastic paraparesis[ncbi.nlm.nih.gov]

  • Plasmablastic Lymphoma

    paraplegia slowly progressing over 2 weeks, along with bowel and bladder involvement.[indianjcancer.com] […] lung, ipsilaterlal moderate pleural effusion, and mediastinal lymphadenopathy P6: A 54-year-old patient with poor compliance to ART presented with fever for 4 months and a spastic[indianjcancer.com]

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