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444 Possible Causes for Huntington's Disease, Small Foot

  • Rett Syndrome

    Eng‐King Tan, Joseph Jankovic and William Ondo, Bruxism in Huntington's disease, Movement Disorders, 15, 1, (171-173), (2001).[doi.org] "In the world of rare diseases, it's quite common, similar in prevalence to Huntington's chorea and in the ball park of cystic fibrosis," said Monica Coenraads, a co-founder[abcnews.go.com]

  • Parkinson's Disease

    Assessment of Caregiver Burden in Huntington's Disease. Yu M, Tan K, Koloms K, Bega D. J Huntingtons Dis. 2019;8(1):111-114. doi: 10.3233/JHD-180326.[parkinsons.northwestern.edu] […] drag small cramped handwriting ( micrographia ) stooped posture trouble sleeping constipation pain decreased sense of smell muscle aches tiredness Depression is common in[medbroadcast.com] Click on the following links to learn more about the conditions we treat: Essential Tremor Huntington's Disease MSA Dystonia PSP Watch this video to learn about focused ultrasound[umm.edu]

  • Autosomal Recessive Spastic Paraplegia Type 20

    When present it is found in distal muscles in the lower limbs, usually the small muscles of the foot and tibialis anterior.[jnnp.bmj.com] […] classified elsewhere G08 Intracranial and intraspinal phlebitis and thrombophlebitis G09 Sequelae of inflammatory diseases of central nervous system G10 Huntington's disease[icd10data.com] HD Chorionzottenbiopsie CVS Chronic granulomatous disease, X-linked CYBB Chronic infections, due to MBL deficiency MBL2 Ciliary dyskinesia, primary RSPH4A Cleidocraniale[meduniwien.ac.at]

  • Early Infantile Epileptic Encephalopathy Type 2

    […] caused by triplet repeat expansion, such as fragile X syndrome (MIM 300624 ) by FMR1 mutation, Huntington disease (HD [MIM 143100 ]) by IT15 mutation, and so on. 21 As seen[ncbi.nlm.nih.gov] disease, Lopes-Maciel-Rodan syndrome (LOMARS) AD/AR 8 7 KCNA2 Epileptic encephalopathy, early infantile AD 15 21 KCNB1 Early infantile epileptic encephalopathy AD 27 30 KCNQ2[blueprintgenetics.com] PHOX2B for congenital central hypoventilation syndrome (CCHS [MIM 209880 ]). 20 Longer expansion of the polyalanine tract causes a more severe phenotype, as well as other diseases[ncbi.nlm.nih.gov]

  • X-linked Parkinsonism-Spasticity Syndrome

    Huntington's disease (also referred to as Huntington's chorea) is an inherited disease that causes certain nerve cells in the brain to degenerate or waste away.[rush.edu] When present it is found in distal muscles in the lower limbs, usually the small muscles of the foot and tibialis anterior.[jnnp.bmj.com] These patients are exquisitely responsive to small doses of levodopa and do not develop motor fluctuations even in advanced disease.[annalsofian.org]

  • Rothmund Thomson Syndrome

    ’s disease, diabetes, Alzheimer’s disease and Parkinson’s disease pathways ( Supplementary Figures S6 and S7 ).[doi.org] […] eyeball 0000568 Osteoporosis 0000939 Short foot Short feet Small feet [ more ] 0001773 Short nose Decreased length of nose Shortened nose [ more ] 0003196 Short palm 0004279[rarediseases.info.nih.gov] […] in all RecQ helicase-deficient cells except RECQL1, including two telomere-related pathways, oxidative phosphorylation and electron transport chain pathways, as well as Huntington’s[doi.org]

  • Sanjad-Sakati Syndrome

    - a lysosomal storage disease Glioblastoma Glycerol kinase deficiency - an X-linked recessive disorder Human papillomavirus E6-induced malignancy Huntington's disease - a[sdbonline.org] foot - Small hand / acromicria - Thin / retracted lips Frequent - Anomalies of teeth and dentition - Enamel anomaly - Repeat respiratory infections Occasional - Anophthalmos[csbg.cnb.csic.es] (very frequent sign) seizures (any type) (very frequent sign) short stature/dwarfism (very frequent sign) small foot (very frequent sign) small hand (very frequent sign) thin[whonamedit.com]

  • Acrootoocular Syndrome

    Holoprosencephaly (Aprosencephaly) Holt-Oram syndrome Homocystinuria Hunter syndrome (MPSII) Huntington Disease Hurler syndrome (MPSI) Hyalanosis Hydranencephaly Hydrocephalus[de.slideshare.net] Disease-Like Syndrome HUPRA Syndrome Hutterite Cerebroosteonephrodysplasia Syndrome hydrolethalus syndrome hypereosinophilic syndrome Hyperimmunoglobulin G1(A1) Syndrome[rgd.mcw.edu] Disease-Like Syndrome HUPRA Syndrome Hutterite Cerebroosteonephrodysplasia Syndrome hydrolethalus syndrome Hydroxylysinuria hypereosinophilic syndrome Hyperimmunoglobulin[rgd.mcw.edu]

  • Spinal and Bulbar Muscular Atrophy

    The Huntington's Disease Collaborative Research Group. 1993.[doi.org] Sensory action potential amplitudes were small.[ncbi.nlm.nih.gov] SBMA belongs to the family of polyglutamine diseases, which also includes Huntington's disease, dentatorubral-pallidoluysian atrophy, and spinocerebellar ataxia (SCA) types[ncbi.nlm.nih.gov]

  • Dementia

    .: Antibodies to Zic4 in paraneoplastic neurologic disorders and small-cell lung cancer. Neurology 2004, 62: 778–782. PubMed Google Scholar 11.[doi.org] Despite the high prevalence of BPSD in progressive neurological diseases (PNDs) such as multiple sclerosis, Huntington's disease, and Parkinson's disease, the utility of a[ncbi.nlm.nih.gov] Dementia can also be caused by Huntington disease, syphilis, multiple sclerosis, acquired immune deficiency syndrome (AIDS), and some types of encephalitis.[britannica.com]

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