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Results 1 - 9 of 9 for Spastic "paraplegia," autosomal dominant
  1. Spastic paraplegia type 8 
    ... Hereditary spastic paraplegia Genetic Testing Registry: Hereditary spastic paraplegia 8 Autosomal dominant spastic paraplegia type 8 Hereditary spastic paraplegia National ...
    https://medlineplus.gov/genetics/condition/spastic-paraplegia-type-8 - Genetics
  2. Spastic paraplegia type 31 
    ... spastic paraplegia 31 Genetic Testing Registry: Hereditary spastic paraplegia Autosomal dominant spastic paraplegia type 31 Hereditary spastic paraplegia National ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-31 - Genetics
  3. Silver syndrome 
    ... spastic paraplegia 17 Genetic Testing Registry: Hereditary spastic paraplegia Autosomal dominant spastic paraplegia type 17 Hereditary spastic paraplegia National ...
    https://medlineplus.gov/genetics/condition/silver-syndrome - Genetics
  4. Spastic paraplegia type 3A 
    ... Hereditary spastic paraplegia Genetic Testing Registry: Hereditary spastic paraplegia 3A Autosomal dominant spastic paraplegia type 3 Hereditary spastic paraplegia National ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-3a - Genetics
  5. Spastic paraplegia type 4 
    ... Organization for Rare Disorders (NORD) ClinicalTrials.gov SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4 PubMed Blackstone C. Hereditary spastic paraplegia. Handb ...
    https://medlineplus.gov/genetics/condition/spastic-paraplegia-type-4 - Genetics
  6. Spastic paraplegia type 7 
    ... symptoms of the condition.In rare cases, spastic paraplegia type 7 is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/genetics/condition/spastic-paraplegia-type-7 - Genetics
  7. Kallmann syndrome 
    ... mutations in other genes, it often has an autosomal dominant pattern of inheritance, which means one copy of ... JP. Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome. Nat Genet. 2003 Apr;33(4): ...
    https://medlineplus.gov/genetics/condition/kallmann-syndrome - Genetics
  8. TUBB4A-related leukodystrophy 
    ... TUBB4A TUBB4A-related leukodystrophy is inherited in an autosomal dominant pattern, which means one copy of the altered ... DN, Kalaydjieva L, Tournev I, Jordanova A. Mosaic dominant TUBB4A mutation in an inbred family with complicated hereditary spastic paraplegia. Mov Disord. 2015 May;30(6):854-8. ...
    https://medlineplus.gov/.../condition/tubb4a-related-leukodystrophy - Genetics
  9. Isolated lissencephaly sequence 
    ... or TUBA1A gene, it is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/.../isolated-lissencephaly-sequence - Genetics