Neurology / Neuropediatrics
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Spastic paralysis, infantile onset ascending (sequence analysis of ALS2 gene)
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Spastic paraplegia 23 | Congenital anomalies of kidney and urinary tract 1 (CAKUT) (deletion/duplication analysis of DSTYK gene)
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Spastic paraplegia 39 | Boucher-Neuhauser syndrome | Oliver-McFarlane syndrome | Laurence-Moon syndrome (deletion/duplication analysis on PNPLA6 gene)
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Spastic paraplegia and psychomotor retardation with or without seizures (deletion/duplication analysis of HACE1 gene)
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Spastic paraplegia type 1 (MASA and CRASH syndrome, sequence analysis of L1CAM gene)
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Spastic paraplegia type 10 (SPG10, sequence analysis of KIF5A gene)
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Spastic paraplegia type 11 (SPG11, deletion/duplication analysis of SPG11 gene)
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Spastic paraplegia type 11 (SPG11, sequence analysis of SPG11 gene)
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Spastic paraplegia type 12 (SPG12, deletion/duplication analysis of RTN2 gene)
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Spastic paraplegia type 12 (SPG12, sequence analysis of RTN2 gene)
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Spastic paraplegia type 13 (SPG13, sequence analysis of HSPD1 gene)
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Spastic paraplegia type 15 (SPG15, sequence analysis of ZFYVE26 gene)
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Spastic paraplegia type 17 (SPG17, sequence analysis of BSCL2 gene)
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Spastic paraplegia type 2, X-linked (SPG2, deletion/duplication analysis on PLP1 gene)
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Spastic paraplegia type 2, X-linked (SPG2, sequence analysis of PLP1 gene)
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Spastic paraplegia type 20 (Troyer syndrome, sequence analysis of SPART gene)
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Spastic paraplegia type 21 (Mast syndrome, sequence analysis of SPG21/ACP33 gene)
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Spastic paraplegia type 26 (SPG26, sequence analysis of B4GALNT1 gene)
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Spastic paraplegia type 28 (SPG28, sequence analysis of DDHD1 gene)
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Spastic paraplegia type 30 (SPG30, deletion/duplication on KIF1A gene)
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