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183 Possible Causes for Allelic Disorder to Parkinson Disease Type 1, Mask-like Facies

  • Dementia with Lewy Bodies

    Despite considerable research to uncover them, the anatomic and neuropathologic correlates of memory impairment in dementia with Lewy bodies (DLB) remain unclear. While some studies have implicated Lewy bodies in the neocortex, others have pointed to α-synuclein pathology in the hippocampus. We systematically[…][ncbi.nlm.nih.gov]

  • Parkinson's Disease

    Facial expression is blunted, described as a "masked facies". The patient typically has difficulty with the initiation of movement.[clinicaladvisor.com] Passive extension and flexion at the elbow can feel like ratcheting, described as cog-wheel rigidity. B.[clinicaladvisor.com]

    Missing: Allelic Disorder to Parkinson Disease Type 1
  • Parkinson's Disease Type 3

    Parkinson's disease type 3 (PD3) is a form of Parkinson's disease that is inherited in an autosomal dominant manner. The underlying mutation has not yet been identified, but PD3 has been related to a 2.5 Mb-locus on the short arm of chromosome 2. To date, PD3 has been diagnosed in distinct families in Europe and[…][symptoma.com]

    Missing: Allelic Disorder to Parkinson Disease Type 1
  • X-linked Parkinsonism-Spasticity Syndrome

    You are using a version of browser that may not display all the features of this website. Please consider upgrading your browser . Format Definition A syndrome characterized by parkinsonian features, such as cogwheel rigidity, resting tremor and bradykinesia, and variably penetrant spasticity. Acronym XPDS[…][uniprot.org]

    Missing: Allelic Disorder to Parkinson Disease Type 1
  • Diffuse Scleroderma

    Chest. 1983 Nov;84(5):546-50. Abstract The pulmonary function and chest roentgenograms were evaluated in 88 patients with the CREST syndrome variant of progressive systemic sclerosis (PSS or scleroderma). Seventy-two percent of the patients had abnormal pulmonary function. An isolated decrease in diffusing[…][ncbi.nlm.nih.gov]

    Missing: Allelic Disorder to Parkinson Disease Type 1
  • Systemic Scleroderma

    Systemic Scleroderma (SSc) is an autoimmune disease that affects connective tissue, resulting in hardening skin, reduced vascular perfusion, gingival fibrosis, enlarged periodontal ligament, xerostomia, and trigeminal neuralgia. Secondary effects, including reduced oral opening and reduced manual dexterity may[…][ncbi.nlm.nih.gov]

    Missing: Allelic Disorder to Parkinson Disease Type 1
  • Limited Cutaneous Systemic Scleroderma

    […] of the skin and limited range of motion Atrophy and necrotic spots Lesions on the proximal nail fold Multiple, painful ischemic digital ulcers Face Loss of expression ( mask-like[amboss.com] facies ) Shortened frenulum Microstomia accompanied with characteristic perioral wrinkles Vascular disease Raynaud's phenomenon Thromboembolism Fatigue, weakness Joint stiffness[amboss.com]

    Missing: Allelic Disorder to Parkinson Disease Type 1
  • Moebius Syndrome

    A case of Möbius' syndrome is presented, with the mask-like facies and poor social relationships consistent with this diagnosis.[ncbi.nlm.nih.gov] A 4-year-old boy presented with mask-like facies noted at birth after a 34-week pregnancy.[ncbi.nlm.nih.gov] The main nerves affected are the sixth (CN VI) and the seventh (CN VII) which results in abnormal gazing and mask like facies.[eyewiki.aao.org]

    Missing: Allelic Disorder to Parkinson Disease Type 1
  • Secondary Myopathy

    BACKGROUND: Some systemic diseases also affect the skeletal muscle to various degrees and with different manifestations. This review aimed at summarizing and discussing recent advances concerning the management of muscle disease in systemic diseases. METHOD: Literature review by search of MEDLINE, and Current[…][ncbi.nlm.nih.gov]

    Missing: Allelic Disorder to Parkinson Disease Type 1
  • Progressive Supranuclear Palsy

    We report a 67-year-old man with 4-repeat (4R) tauopathy sharing both features of corticobasal degeneration (CBD) and progressive supranuclear palsy (PSP). Although CBD and PSP have a common pathological feature that 4R tau accumulates in neurons and glia, recent pathological studies have confirmed[…][ncbi.nlm.nih.gov]

    Missing: Allelic Disorder to Parkinson Disease Type 1

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