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1,045 Possible Causes for Caused by Mutation in the DMX-like 2 Gene (DMXL2), Pyramidal Syndrome

Did you mean: Caused by Mutation in the DMX-like 2 Gene (DMXL2, Pyramidal Syndrome

  • Pallidopyramidal Syndrome

    Homepage Rare diseases Search Search for a rare disease Parkinsonian-pyramidal syndrome Disease definition Parkinsonian-pyramidal syndrome is a rare, genetic, neurological[orpha.net] […] parkinsonian-pyramidal syndrome since the first description by Davison in 1954.[moh-it.pure.elsevier.com] ORPHA:171695 Synonym(s): Pallidopyramidal syndrome Prevalence: - Inheritance: Autosomal recessive Age of onset: Adolescent, Adult ICD-10: G20 OMIM: 168100 168601 260300 UMLS[orpha.net]

    Missing: Caused by Mutation in the DMX-like 2 Gene (DMXL2)
  • Polyendocrine - Polyneuropathy Syndrome

    […] hypogonadism, incomplete puberty, progressive non-autoimmune insulin-dependent diabetes mellitus, peripheral demyelinating sensorimotor polyneuropathy, and cerebellar and pyramidal[malacards.org] […] by mutation in the DMX-like 2 gene (DMXL2, 612186.0001) Description Hall (1965) described 5 families in which 14 cases of myxedema occurred in addition to the 5 probands.[findzebra.com] MalaCards based summary : Polyendocrine-Polyneuropathy Syndrome, is also known as pepns , and has symptoms including ataxia An important gene associated with Polyendocrine-Polyneuropathy[malacards.org]

  • Pyramidal Tract Disorder

    Definition A pyramidal syndrome attacks the pyramidal tracts, the neural pathways controlling voluntary movement.[health.ccm.net] Drugs that are associated with Pyramidal tract syndrome Pyramidal tract syndrome (168 drugs) Could your condition cause Pyramidal tract syndrome Pyramidal tract syndrome ([ehealthme.com] Synonyms (terms occurring on more labels are shown first): pyramidal tract syndrome More information : PubMed search and possibly Wikipedia License: Except as otherwise noted[sideeffects.embl.de]

    Missing: Caused by Mutation in the DMX-like 2 Gene (DMXL2)
  • Juvenile Paralysis Agitans of Hunt

    Syndrome [7] occuring in families.[neurologyindia.com] Syndrome, Parkinsonian-pyramidal syndrome, pallidopyramidal syndrome, Pallidopyramidal Syndrome, PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET, Pallidopyramidal syndrome[monarchinitiative.org] Pallido-pyramidal syndrome. J Neuropath Exp Neurol 1954, 13: 50. [ Links ] 7. Drayer BP. Magnetic resonance imaging and extrapyramidal movement disorders.[scielo.br]

    Missing: Caused by Mutation in the DMX-like 2 Gene (DMXL2)
  • Pharyngitis

    […] headache, weakness, fatigue, restlessness, sedation, insomnia, mood changes, agitation, personality disorder, impaired speech, tardive dyskinesia, dystonia, tremor, extra-pyramidal[medical-dictionary.thefreedictionary.com] […] effects, neuroleptic malignant syndrome, coma, postinjection delirium-sedation syndrome CV: orthostatic hypotension, chest pain, tachycardia EENT: amblyopia, rhinitis, pharyngitis[medical-dictionary.thefreedictionary.com]

    Missing: Caused by Mutation in the DMX-like 2 Gene (DMXL2)
  • Pyramidal Tract Lesion

    […] is gradual, but all the cardinal signs of the pyramidal syndrome eventually appear 18 .[jneurology.com] Synonyms (terms occurring on more labels are shown first): pyramidal tract syndrome More information : PubMed search and possibly Wikipedia License: Except as otherwise noted[sideeffects.embl.de] Second patient had findings of left pyramidal syndrome. ... -------------------------------------------------- Note added at 7 mins (2005-08-08 16:32:23 GMT) -------------[proz.com]

    Missing: Caused by Mutation in the DMX-like 2 Gene (DMXL2)
  • Behr Syndrome

    In the second decade, they gradually developed gait difficulties due to a moderate spastic pyramidal syndrome and mild cerebellar ataxia.[doi.org] Behr syndrome was first described in 1909 as a syndrome of heredofamilial optic atrophy, visual disturbances, nystagmus, and variable pyramidal tract signs.[ncbi.nlm.nih.gov] A 6-year-old girl with a progressive syndrome of optic atrophy, ataxia, myoclonic epilepsy, urinary incontinence, and pyramidal tract degeneration suggestive of Behr syndrome[ncbi.nlm.nih.gov]

    Missing: Caused by Mutation in the DMX-like 2 Gene (DMXL2)
  • T3 Thyrotoxicosis

    The authors concluded that the left pyramidal syndrome was secondary to autoimmune free T3-thyrotoxicosis.[ncbi.nlm.nih.gov]

    Missing: Caused by Mutation in the DMX-like 2 Gene (DMXL2)
  • Puerperium

    It was initially described in Mexican families presenting with ataxia and epilepsy, with or without polyneuropathy, pyramidal signs and cognitive symptoms.[ncbi.nlm.nih.gov] The authors report three patients from the same family who were asymptomatic until gestation and puerperium, when they developed symptoms and signs suggestive of the syndrome[ncbi.nlm.nih.gov]

    Missing: Caused by Mutation in the DMX-like 2 Gene (DMXL2)
  • Infantile-Onset Ascending Hereditary Spastic Paralysis

    syndrome - Speech troubles / aphasia / dysphasia / echolalia / mutism / logorrhea / dysprosodia Frequent - Abnormal eye movements / oculomotor disorder - Pseudobulbar signs[csbg.cnb.csic.es] […] variant of Guillain-Barré syndrome Paraplegia-intellectual disability-hyperkeratosis syndrome Parkinsonian-pyramidal syndrome Parkinsonism with dementia of Guadeloupe Paroxysmal[se-atlas.de] Conditions combining a bilateral pyramidal syndrome with limb and bulbar amyotrophy.[cmm.ucsd.edu]

    Missing: Caused by Mutation in the DMX-like 2 Gene (DMXL2)

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