Create issue ticket

155 Possible Causes for Difficulty Climbing Stairs, Hypomyelination

  • Arthritis

    Stowe and Lakshmi Raman, Perinatal chronic hypoxia induces cortical inflammation, hypomyelination, and peripheral myelin‐specific T cell autoreactivity, Journal of Leukocyte[doi.org] Among adults with arthritis, six million are limited in social activities, eight million have difficulty climbing stairs, and 11 million have difficulty walking short distances[arthritis.about.com] […] with movement in general and doing any of the follow activities: Walking Climbing stairs Lifting objects Grasping or holding objects Doing intricate, detailed work, such[draxe.com]

  • Limb-Girdle Muscular Dystrophy Type 1E

    […] neuropathy-arthrogryposis syndrome Hypomyelination-congenital cataract syndrome Hypophosphatasia Hypophosphatemic rickets Hypoplastic tibiae-postaxial polydactyly syndrome[se-atlas.de] LGMD1 patients may need to use walking aids, can have difficulties climbing stairs and lose the ability to walk.[mdfgauteng.org] Symptoms that might be noticed first include frequent falls and difficulty climbing stairs, running and rising from the floor.[mda.org.au]

  • Limb-Girdle Muscular Dystrophy Type 2L

    stairs.[egl-eurofins.com] Gene Diseases External Disease Links POLR3B Hypomyelinating leukodystrophy 8 GHR GeneReviews OMIM POMGNT1 Congenital muscular dystrophy-dystroglycanopathy with mental retardation[genepeeks.com] climbing stairs and walking.[rarediseases.org]

  • Diabetic Amyotrophy

    A steady decline led to mobilisation with a Zimmer frame and great difficulty climbing stairs.[pmj.bmj.com] Congenital hypomyelinating neuropathy Congenital hypomyelinating neuropathy. The Schwann cell touches the axon but makes no myelin. There are rings of basement membrane.[neuropathology-web.org] climbing stairs.[e-arm.org]

  • Muscular Dystrophy-Dystroglycanopathy Type B5

    […] neuropathy (CHN), Neuropathy, congenital hypomyelinating, CMT4E, Hypomyelination, severe congenital, CHN, Charcot Marie Tooth disease type 4E, Autosomal recessive congenital[rarediseases.info.nih.gov] , 2 1 Leukodystrophy, Hypomyelinating, 4 1 Leukoencephalopathy With Vanishing White Matter 9 Leydig Cell Hypoplasia, Type I 1 Li-Fraumeni Syndrome 15 Li-Fraumeni Syndrome[preventiongenetics.com] hypomyelinating neuropathy, Congenital hypomyelination neuropathy Congenital fiber type disproportion Synonyms: Congenital fiber-type disproportion myopathy, Myopathy, congenital[rarediseases.info.nih.gov]

  • Limb-Girdle Muscular Dystrophy Type 2J

    […] leukodystrophy with or without oligondontia and/or hypogonadism Hypomyelinating leukodystrophy-ataxia-hypodontia-hypomyelination syndrome Hypomyelination with atrophy of[se-atlas.de] LGMD1 patients may need to use walking aids, can have difficulties climbing stairs and lose the ability to walk.[mdfgauteng.org] climbing stairs Difficulty walking up stairs 0003551 Difficulty running 0009046 Dilated cardiomyopathy Stretched and thinned heart muscle 0001644 Frequent falls 0002359 Motor[rarediseases.info.nih.gov]

  • Muscular Dystrophy-Dystroglycanopathy Type C9

    […] neuropathy-arthrogryposis syndrome Hypomyelination-congenital cataract syndrome Hypophosphatasia Hypophosphatemic rickets Hypoplastic tibiae-postaxial polydactyly syndrome[se-atlas.de] LGMD1 patients may need to use walking aids, can have difficulties climbing stairs and lose the ability to walk.[mdfgauteng.org] climbing stairs and walking.[rarediseases.org]

  • Muscular Dystrophy-Dystroglycanopathy Type C2

    […] neuropathy-arthrogryposis syndrome Hypomyelination-congenital cataract syndrome Hypophosphatasia Hypophosphatemic rickets Hypoplastic tibiae-postaxial polydactyly syndrome[se-atlas.de] LGMD1 patients may need to use walking aids, can have difficulties climbing stairs and lose the ability to walk.[mdfgauteng.org] climbing stairs and walking.[rarediseases.org]

  • Muscular Dystrophy-Dystroglycanopathy Type C12

    @article{Renesse2014POMKMI, title {POMK mutation in a family with congenital muscular dystrophy with merosin deficiency, hypomyelination, mild hearing deficit and intellectual[semanticscholar.org] climbing stairs EMG: myopathic abnormalities Congenital muscular dystrophy Spinal rigidity Cardiomyopathy Toe walking Motor delay Scapular winging Trophic changes related[mendelian.co] (PMID: 23519211) Jae LT … Brummelkamp TR (Science (New York, N.Y.) 2013) 2 3 4 60 POMK mutation in a family with congenital muscular dystrophy with merosin deficiency, hypomyelination[genecards.org]

  • Charcot-Marie-Tooth Disease Type 2S

    […] axonal neuropathy (Gigaxonin) CMT 3 (PMP22, MPZ, PRX, ERG2) CMT 4 ( GDAP1 , MTM2, MTM13, SH3TC2, NDRG1, ERG2, PRX, HK1, FDG4, FIG4) CMTX 2 (Xp22.2) CMTX 4 (AIFM1) Congenital hypomyelination[neuromuscular.wustl.edu] climbing stairs.[paleyinstitute.org] […] or Amyelinating, Autosomal Recessive Charcot-Marie-Tooth Disease, Type 4e Charcot-Marie-Tooth Neuropathy, Type 4e Congenital Hypomyelinating Neuropathy Hypomyelination, Severe[ukgtn.nhs.uk]

Further symptoms

Similar symptoms