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642 Possible Causes for Progressive Hearing Loss, Progressive Muscle Weakness

  • Autosomal Dominant Progressive External Ophthalmoplegia Type 3

    Loss (Chronic) Progressive External Ophthalmoplegia Maternal Myopathy and Cardiomyopathy Maternally Inherited Hypertrophic Cardiomyopathy Maternally Inherited Cardiomyopathy[] Patients with C10ORF2-linked Autosomal dominant Progressive external ophthalmoplegiamay have other Clinical features including proximal Muscle weakness, ataxia, peripheral[] Additional signs and symptoms can include hearing loss caused by nerve damage in the inner ear (sensorineural hearing loss), weakness and loss of sensation in the limbs due[]

  • Dementia

    loss] or cognitive impairment from medicines associated with increased anticholinergic burden) have been investigated and dementia is still suspected. 1.2.7 If the person[] In vascular dementia, the first symptoms are often the neurological ones, such as problems with reflexes, walking, and muscle weakness.[] […] has suspected rapidly-progressive dementia, refer them to a neurological service with access to tests (including cerebrospinal fluid examination) for Creutzfeldt–Jakob disease[]

  • Lethal Ataxia with Deafness and Optic Atrophy

    […] with peripheral or optic neuropathy, prelingual progressive sensorineural hearing loss, and central nervous system impairment.[] […] myoclonic epilepsy • action induced polymyoclonus • ataxia Late Symptoms • progressive muscle weakness and atrophy • hypertrophic cardiomyopathy • dementia • deafness • multiple[] However, recurrent infections in childhood leading to acute deteriorations of slowly progressive muscle weakness, severe ataxia leading to walker-dependency, mild to moderate[]

  • Autosomal Dominant Progressive External Ophthalmoplegia

    Additional symptoms are variable, and may include cataracts, hearing loss, sensory axonal neuropathy, ataxia, depression, hypogonadism, and parkinsonism.[] weakness ; Multiple mitochondrial DNA deletions ; Myalgia ; Progressive ; Progressive external ophthalmoplegia ; Progressive muscle weakness ; Ptosis ; Seizures ; Variable[] Acronym PEOA2 Synonyms Chronic progressive external ophthalmoplegia CPEO Graefe disease Mitochondrial ocular myopathy Ocular myopathy of von Graefe-Fuchs Progressive external[]

  • Mitochondrial Myopathy and Sideroblastic Anemia

    […] impairment, ranging from profound congenital deafness to severe and moderate progressive hearing loss of late onset or to completely normal hearing.[] Affected individuals manifest progressive muscle weakness, exercise intolerance, lactic acidosis, sideroblastic anemia and delayed growth.[] Mitochondrial neurogastrointestinal encephalomyopathy associated with progressive hearing loss. J Laryngol Otol . 2010;124:1007–1009. 86.[]

  • Amish Nemaline Myopathy

    […] kyphoscoliosis, myopathy, and hearing loss,614557 FKRP930.990.98Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5613153 FKRP930.990.98Muscular[] The muscle weakness tends to progress slowly and many patients can live independent lives.[] , and tremors, and then progressive muscle weakness, a severely deformed chest, muscle wasting, and life-threatening respiratory insufficiency How is nemaline myopathy diagnosed[]

  • Muscular Dystrophy

    An infant-onset form of FSHD can also cause retinal disease and some hearing loss.[] Abstract Muscular dystrophy (MD) is a group of progressive muscle weakness diseases.[] Affected individuals have severe progressive proximal muscle weakness.[]

  • Polyendocrine - Polyneuropathy Syndrome

    […] developmental delay and Progressive hearing impairment that can help you solving undiagnosed cases.[] DFNA71 is characterized by bilateral mild to moderate hearing loss before age 20 years, which gradually progresses to severe to profound hearing loss.[] muscle disorder that often starts with weakness in the hands.[]

  • Glycogen Storage Disease Type 2

    loss.[] It is characterized by delayed motor skills (such as rolling over and sitting) and progressive muscle weakness.[] The sixth patient was started on treatment at 14 months of age because of progressive muscle weakness.[]

  • Usher Syndrome Type 3B

    Definition A syndrome characterized by progressive vision and hearing loss during early childhood.[] […] distal muscle weakness and atrophy.[] Usher syndrome type III is characterized by postlingual, progressive hearing loss, variable vestibular dysfunction, and onset of retinitis pigmentosa symptoms, including nyctalopia[]

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