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480 Possible Causes for Tongue Weakness, Vacuolization

  • Oculo-Pharyngo-Distal Myopathy

    Muscular dystrophy changes with rimmed vacuoles were the main histopathological changes.[] […] muscles Bulbar Dysphagia: Oropharyngeal Dysarthria: Hoarse & Nasal voice Tongue weakness Limbs Legs Arms Distal: Anterior tibial; Finger extensors Onset: 5 years after disease[] Myopathological findings showed rimmed vacuoles with varying degrees of muscular dystrophic changes.[]

  • Oculopharyngeal Muscular Dystrophy

    In contrast, patients with distal myopathy with rimmed vacuoles revealed many rimmed vacuoles, on average in 20% of the fibers, and their oculopharyngeal muscles were spared[] Symptoms may include: difficulty swallowing (dysphagia) tongue weakness and atrophy weakness in the proximal muscles drooping eyelids (ptosis) difficulty gazing upwards and[] The following are some of the associated symptoms of OPMD: Drooping eyelids (ptosis) Difficulty swallowing (dysphagia) Atrophy of the tongue Weakness of the muscles in the[]

  • Distal Myopathy Type 3

    Tubulofilamentous inclusion, myeloid bodies, and autophagic vacuoles in the area corresponding to rimmed vacuoles ( d ; bar 1 μm).[] (ie, tongue and pharyngeal weakness) is manifested by symptoms of dysarthria and dysphagia.[] Yonsei Medical Journal. 2013; 54(3): 578-582 [Pubmed] 7 Distal myopathy with rimmed vacuoles and inflammation: A genetically proven case Kannan, M.A. and Challa, S. and Urtizberea[]

  • Limb-Girdle Muscular Dystrophy Type 2G

    Frequent rimmed vacuoles were observed.[] Involvement of the heart, respiratory muscles or tongue. (Facial weakness is not usual.)[] LGMD2G (telethoninopathy) This form of LGMD usually becomes apparent during childhood or adolescence and presents with muscle weakness of the upper and lower legs.[]

  • Progressive Bulbar Palsy

    IVIg) Myopathies, including inclusion body myositis, which is characterized by wasting and weakness of deep finger flexors and the quadriceps femoris with typical rimmed vacuoles[] Clinical manifestations include dysarthria, dysphagia, facial weakness, tongue weakness, and fasciculations of the tongue and facial muscles.[] A motor neuron disease marked by progressive weakness of the muscles innervated by cranial nerves of the lower brain stem.[]

  • Sarcotubular Myopathy

    The vacuoles are similar to those described in sarcotubular myopathy. TRIM32 sequencing revealed the common c.1459G A mutation at homozygosity.[] Patients may have prominent tongue hypertrophy and severe weakness and wasting of upper arms, neck flexors, and axial muscles; these features can help in distinguishing this[] Myriad small spaces appeared in abnormal fibers in the transverse sections, while in longitudinal sections the vacuolation was segmental in distribution.[]

  • Limb-Girdle Muscular Dystrophy

    […] pathology Vacuoles/ultrastructure Substances Chromatin LMNA protein, human Lamin Type A MyoD Protein MyoD1 myogenic differentiation protein PAX7 Transcription Factor PAX7[] Involvement of the heart, respiratory muscles or tongue. (Facial weakness is not usual.)[] Our case suggests that posterior-dominant lower limb muscle impairment with gluteus and truncal muscle involvement and the detection of rimmed vacuoles on a muscle biopsy[]

  • Autosomal Recessive Limb-Girdle Muscular Dystrophy

    Histopathology of skeletal muscles biopsies showed typical dystrophic changes with many rimmed vacuoles.[] Involvement of the heart, respiratory muscles or tongue. (Facial weakness is not usual.)[] […] sibs from one of them (family LG61) revealed some clinical and laboratory findings (early involvement of the distal muscles, mildly elevated serum CK levels, and rimmed vacuoles[]

  • Hereditary Proximal Myopathy with Early Respiratory Failure

    TDP43 immunoreactivity was observed adjacent to rimmed vacuoles and in areas around cytoplasmic bodies.[] Other regions: Some patients Cranial nerves: Face; Tongue Posterior neck : Head ptosis Back: Camptocormia Asymmetric : Often Progression Slow: Over 1 to 2 decades To severe[] ; DMRV; Nonaka myopathy; Rimmed vacuole myopathy; Quadriceps Sparing Myopathy; GNE myopathy "OMIM Entry # 605820 - Nonaka Myopathy".[]

  • Beta-Mannosidosis

    There were no detectable oligosaccharides or cytoplasmic vacuolation in the liver or spleen.[] Signs and symptoms of Alpha-Mannosidosis include: Intellectual disability Reduced bone density, muscular weakness Spine deformations Bowed legs Prominent forehead, low hairline[] Electron microscopy of skin biopsy specimens from the patient showed cytoplasmic vacuolation of lysosomes in blood and lymph vessels, endothelial cells, fibroblasts, secretory[]

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