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6 Possible Causes for Lower Limb Muscle Atrophy due to Peripheral Neuropathy

  • Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1H

    […] by distal sensory impairment predominantly affecting the lower limbs and resulting in walking difficulties due to muscle weakness and atrophy.[mendelian.co] Learn more Other less relevant matches: Low match CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE C; CMTRIC CMTRIC is an autosomal recessive peripheral neuropathy characterized[mendelian.co]

  • Autosomal Recessive Spastic Paraplegia Type 26

    […] to lower limb spasticity and muscle weakness.[malacards.org] SPG26 is a complicated form characterized by onset in the first 2 decades of life of gait abnormalities due to lower limb spasticity and muscle weakness.[malacards.org] Additional features include intellectual disability, peripheral neuropathy, dysarthria, cerebellar signs, extrapyramidal signs, and cortical atrophy.[malacards.org]

  • Autosomal Recessive Spastic Paraplegia 52

    SPG26 is a complicated form characterized by onset in the first 2 decades of life of gait abnormalities due to lower limb spasticity and muscle weakness.[malacards.org] Additional features include intellectual disability, peripheral neuropathy, dysarthria, cerebellar signs, extrapyramidal signs, and cortical atrophy.[malacards.org] OMIM : 58 SPG26 is an autosomal recessive form of complicated spastic paraplegia characterized by onset in the first 2 decades of life of gait abnormalities due to lower limb[malacards.org]

  • Autosomal Dominant Centronuclear Myopathy

    neuropathy characterized by distal sensory impairment predominantly affecting the lower limbs and resulting in walking difficulties due to muscle weakness and atrophy.[mendelian.co] Top matches: Low match CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE A; CMTRIA Autosomal recessive intermediate Charcot-Marie-Tooth disease A (CMTRIA) is a peripheral[mendelian.co]

  • Distal Sensory Loss (all Modalities)

    […] characterized by distal sensory impairment predominantly affecting the lower limbs and resulting in walking difficulties due to muscle weakness and atrophy.[ncbi.nlm.nih.gov] Charcot-Marie-Tooth disease, recessive intermediate c MedGen UID: 815639 • Concept ID: C3809309 • Disease or Syndrome CMTRIC is an autosomal recessive peripheral neuropathy[ncbi.nlm.nih.gov]

  • Spastic Paraplegia - Ataxia - Mental Retardation

    […] to lower limb spasticity and muscle weakness.[ncbi.nlm.nih.gov] Additional features include intellectual disability, peripheral neuropathy, dysarthria, cerebellar signs, extrapyramidal signs, and cortical atrophy.[ncbi.nlm.nih.gov] • Disease or Syndrome SPG26 is an autosomal recessive form of complicated spastic paraplegia characterized by onset in the first 2 decades of life of gait abnormalities due[ncbi.nlm.nih.gov]

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