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Results 1 - 8 of 8 for Autosomal recessive lower motor neuron disease with childhood onset
  1. Troyer syndrome 
    ... not show signs and symptoms of the condition. Autosomal recessive spastic paraplegia type 20 Spastic paraparesis, childhood-onset, with distal muscle wasting Spastic paraplegia 20, autosomal ...
    https://medlineplus.gov/genetics/condition/troyer-syndrome - Genetics
  2. Muscular Dystrophy From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Muscular Dystrophy/Start Here ... Muscular Dystrophy ... National Institute of Neurological Disorders and Stroke ... Muscular dystrophy (MD) refers to a group of genetic ...
    https://www.ninds.nih.gov/.../disorders/muscular-dystrophy - External Health Links
  3. Lipid Storage Diseases From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Leukodystrophies/Specifics ... Leukodystrophies ... Genetic Brain Disorders/Specifics ... Genetic Brain Disorders ... Tay-Sachs Disease/Related Issues ... Tay-Sachs Disease ... Lipid ...
    https://www.ninds.nih.gov/.../disorders/lipid-storage-diseases - External Health Links
  4. Sandhoff disease 
    ... genes. HEXB This condition is inherited in an autosomal recessive pattern, which means both copies of the gene ... variants. The parents of an individual with an autosomal recessive condition each carry one copy of the altered ...
    https://medlineplus.gov/genetics/condition/sandhoff-disease - Genetics
  5. Charcot-Marie-Tooth Disease From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Charcot-Marie-Tooth Disease/Start Here ... Charcot-Marie-Tooth Disease ... National Institute of Neurological Disorders and Stroke ... Charcot-Marie-Tooth disease (CMT) ...
    https://www.ninds.nih.gov/.../disorders/charcot-marie-tooth-disease - External Health Links
  6. Spinal muscular atrophy 
    ... SMN2 Spinal muscular atrophy is inherited in an autosomal recessive pattern, which means both copies of the SMN1 ... cases, the parents of an individual with an autosomal recessive condition each carry one copy of the mutated ...
    https://medlineplus.gov/genetics/condition/spinal-muscular-atrophy - Genetics
  7. Riboflavin transporter deficiency neuronopathy 
    ... SLC52A3 Riboflavin transporter deficiency neuronopathy usually follows an autosomal recessive pattern of inheritance, which means both copies of ... mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated ...
    https://medlineplus.gov/...lavin-transporter-deficiency-neuronopathy - Genetics
  8. Describing SMA (Cure SMA)  
    Spinal Muscular Atrophy/Start Here ... Spinal Muscular Atrophy ... Make today a breakthrough. No two people with spinal muscular atrophy (SMA) have identical experiences. ...
    https://www.curesma.org/describing-sma - External Health Links