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2,312 Possible Causes for Agenesis of the Occipital Lobes, Progressive Muscle Weakness

  • Congenital Muscular Dystrophy

    Abstract Congenital muscular dystrophies (CMD) cause progressive muscle weakness resulting in severe motor disabilities.[ncbi.nlm.nih.gov] Uncommonly, agenesis of septum pellucidum can be seen. Polymicrogyria typically seen in the frontal and parietal lobes.[neuroradiologycases.com] Abstract A 6-year-old boy born by a third-degree consanguineous marriage presented with progressive muscle weakness and delayed motor milestones noticed in early infancy with[ncbi.nlm.nih.gov]

  • Muscular Dystrophy

    Abstract Muscular dystrophy (MD) is a group of progressive muscle weakness diseases.[ncbi.nlm.nih.gov] muscle weakness, and rarely by alopecia.[ncbi.nlm.nih.gov] Symptoms The main sign of muscular dystrophy is progressive muscle weakness.[mayoclinic.org]

    Missing: Agenesis of the Occipital Lobes
  • Amish Nemaline Myopathy

    […] neonatal onset 0001319 Pectus carinatum Pigeon chest 0000768 Progressive muscle weakness 0003323 Proximal amyotrophy 0007126 Shoulder flexion contracture 0003044 Tremor Tremors[rarediseases.info.nih.gov] The muscle weakness tends to progress slowly and many patients can live independent lives.[thinkgenetic.com] , and tremors, and then progressive muscle weakness, a severely deformed chest, muscle wasting, and life-threatening respiratory insufficiency How is nemaline myopathy diagnosed[patientworthy.com]

    Missing: Agenesis of the Occipital Lobes
  • Duchenne Muscular Dystrophy

    English Duchenne muscular dystrophy Duchenne muscular dystrophy (DMD) is a neuromuscular disease characterized by rapidly progressive muscle weakness and wasting due to degeneration[wikidata.org] Because of the progressive muscle weakness they experience, patients with Duchenne muscular dystrophy frequently utilize positive-pressure devices to maintain adequate bronchial[ncbi.nlm.nih.gov] Progressive, Duchenne Type DMD Duchenne Muscular Dystrophy MUSCULAR DYSTROPHY, DUCHENNE TYPE[wikidata.org]

    Missing: Agenesis of the Occipital Lobes
  • Inclusion Body Myositis

    It is characterized by slowly progressive muscle weakness and atrophy, with typical pathological changes of inflammation, degeneration and mitochondrial abnormality in affected[ncbi.nlm.nih.gov] An inflammatory myopathy, inclusion body myositis (IBM) presents with progressive muscle weakness against a background of elevated creatine kinase and diffuse endomysial damage[ncbi.nlm.nih.gov] Inclusion body myositis (IBM), a condition characterised by progressive muscle weakness and inclusion bodies visible on muscle biopsy, is the most common type of myopathy[ncbi.nlm.nih.gov]

    Missing: Agenesis of the Occipital Lobes
  • Lethal Ataxia with Deafness and Optic Atrophy

    During infection, the slowly progressive muscle weakness is punctuated by acute deterioration in muscle strength, which may result in respiratory failure requiring mechanical[ncbi.nlm.nih.gov] However, recurrent infections in childhood leading to acute deteriorations of slowly progressive muscle weakness, severe ataxia leading to walker-dependency, mild to moderate[doi.org] […] myoclonic epilepsy • action induced polymyoclonus • ataxia Late Symptoms • progressive muscle weakness and atrophy • hypertrophic cardiomyopathy • dementia • deafness • multiple[emilytam.com]

    Missing: Agenesis of the Occipital Lobes
  • Glycogen Storage Disease Type 2

    It is characterized by delayed motor skills (such as rolling over and sitting) and progressive muscle weakness.[ghr.nlm.nih.gov] The sixth patient was started on treatment at 14 months of age because of progressive muscle weakness.[ncbi.nlm.nih.gov] Most individuals with late-onset Pompe disease experience progressive muscle weakness, especially in the legs and the trunk, including the muscles that control breathing.[ghr.nlm.nih.gov]

    Missing: Agenesis of the Occipital Lobes
  • Becker Muscular Dystrophy

    From Wikidata Jump to navigation Jump to search X-linked recessive inherited disorder characterized by slowly progressive muscle weakness of the legs and pelvis Benign pseudohypertrophic[wikidata.org] Becker muscular dystrophy (BMD), a genetic disorder of X-linked recessive inheritance, typically presents with gradually progressive muscle weakness.[ncbi.nlm.nih.gov] Becker muscular dystrophy (BMD) is characterized by progressive muscle weakness.[ncbi.nlm.nih.gov]

    Missing: Agenesis of the Occipital Lobes
  • Progressive Muscular Atrophy

    This results in progressive muscle weakness, fasciculations (rippling effect under the skin), and shrinkage in muscle bulk and weight loss.[umcutrecht.nl] Symptoms The main sign of muscular dystrophy is progressive muscle weakness.[mayoclinic.org] Individuals may experience progressive muscle weakness in the muscles closest to the center of the body, such as the shoulders, thighs, and pelvis.[togetherinsma.com]

    Missing: Agenesis of the Occipital Lobes
  • Limb-Girdle Muscular Dystrophy

    Here we describe a 35-years-old who experienced progressive muscle weakness.[ncbi.nlm.nih.gov] Abstract Patients with Limb girdle muscular dystrophy type 2I (LGMD2I) are characterized by progressive muscle weakness and wasting primarily in the proximal muscles, while[ncbi.nlm.nih.gov] Abstract Recessive limb-girdle muscular dystrophies (LGMD2) involve progressive muscle weakness.[ncbi.nlm.nih.gov]

    Missing: Agenesis of the Occipital Lobes

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