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Zaniki mięśni pochodzenia rdzeniowego – zróżnicowana klinicznie i genetycznie grupa chorób rzadkich, których cechą wspólną jest degeneracja neuronów ruchowych i postępujące upośledzenie różnych grup mięśniowych w organizmie.
, Spinal muscular atrophies (SMAs) are a gen … Spinal muscular atrophies (SMAs) are a genetically and clinically heterogeneous group of rare debilitating disorders characterised by the degeneration of lower motor neurons (neuronal cells situated in the anterior horn of the spinal cord) and subsequent atrophy (wasting) of various muscle groups in the body. While some SMAs lead to early infant death, other diseases of this group permit normal adult life with only mild weakness.normal adult life with only mild weakness.
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| rdfs:comment |
Spinal muscular atrophies (SMAs) are a gen … Spinal muscular atrophies (SMAs) are a genetically and clinically heterogeneous group of rare debilitating disorders characterised by the degeneration of lower motor neurons (neuronal cells situated in the anterior horn of the spinal cord) and subsequent atrophy (wasting) of various muscle groups in the body. While some SMAs lead to early infant death, other diseases of this group permit normal adult life with only mild weakness.normal adult life with only mild weakness.
, Zaniki mięśni pochodzenia rdzeniowego – zróżnicowana klinicznie i genetycznie grupa chorób rzadkich, których cechą wspólną jest degeneracja neuronów ruchowych i postępujące upośledzenie różnych grup mięśniowych w organizmie.
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Spinal muscular atrophies
, Zaniki mięśni pochodzenia rdzeniowego
|
