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paraplégia spastická dedičná

  1. Record numberd015419
    Date06.06.2025
    TypeM
    Topical termparaplégia spastická dedičná
    Other termEnglish (Pseudonym) Autosomal Recessive Spastic Paraplegia
    English (Pseudonym) Autosomal Dominant Hereditary Spastic Paraplegia
    English (Pseudonym) Hereditary Spastic Paraplegia
    English (Pseudonym) Charcot-Marie-Tooth Disease with Pyramidal Features, Autosomal Dominant
    English (Pseudonym) Spastic Paraplegia Type 5A, Recessive
    English (Pseudonym) Spastic Paraplegia Type 2
    English (Pseudonym) Hereditary Motor and Sensory Neuropathy 5
    English (Pseudonym) Hereditary Motor-Sensory Neuropathy with Pyramidal Signs
    English (Pseudonym) X-Linked, Spastic Paraplegia, Hereditary
    English (Pseudonym) Peroneal Muscular Atrophy with Pyramidal Features, Autosomal Dominant
    Slovak (Pseudonym) paraplégia spastická hereditárna
    Slovak (Pseudonym) paraplégia spastická, autozomálne recesívna
    Slovak (Pseudonym) paraplégia spastická, autozomálne dominantná
    Slovak (Pseudonym) Charcot-Marie-Toothova choroba s pyramídovými znakmi, autozomálne dominantná
    Slovak (Pseudonym) neuropatia hereditárna motorická a senzorická, typ 5
    Slovak (Pseudonym) neuropatia dedičná, motoricko-senzorická s pyramídovými znakmi
    Slovak (Pseudonym) paraplégia spastická dedičná, viazaná na X chromozóm
    Slovak (Pseudonym) paraplégia spastická typ 2
    Slovak (Pseudonym) paraplégia spastická typ 5A, recesívna
    Slovak (Pseudonym) atrofia peroneálna svalová s pyramídovými znakmi, autozomálne dominantná
    UDCC10.500.300.820C10.574.500.495.820C10.668.829.800.300.820C16.131.666.300.820C16.320.400.375.820
    NoteA group of inherited diseases that share similar phenotypes but are genetically diverse. Different genetic loci for autosomal recessive, autosomal dominant, and x-linked forms of hereditary spastic paraplegia have been identified. Clinically, patients present with slowly progressive distal limb weakness and lower extremity spasticity. Peripheral sensory neurons may be affected in the later stages of the disease. (J Neurol Neurosurg Psychiatry 1998 Jan;64(1):61-6; Curr Opin Neurol 1997 Aug;10(4):313-8)
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Number of the records: 1  

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