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105 Possible Causes for Facial Muscle Weakness and Progressive Atrophy, Rapid Progression

  • Autosomal Recessive Lower Motor Neuron Disease with Childhood Onset

    Disease progression was rapid, and the majority of patients died from respiratory failure within 1–5 years after onset of disease.[link.springer.com] Spinal muscular atrophy is characterised by slowly progressive muscle weakness and atrophy of the limb muscles associated with motor neurone loss in the spinal cord.[patient.info] Hereditary pure lower motor neuron disease with adult onset and rapid progression. J Neurol 2001 ; 248 : 290 –96.[academic.oup.com]

  • Progressive Muscular Atrophy

    Rapid progression and typical ubiquitinated inclusions in lower motor neurons were present in 77 (95%) of the cases.[ncbi.nlm.nih.gov] Symptoms include pharyngeal muscle weakness (involved with swallowing), weak jaw and facial muscles, progressive loss of speech, and tongue muscle atrophy.[web.archive.org] Kovacs, Sandor Czirjak, Peter Pusztai, Ibolya Varga and Karoly Racz, Rapid Progression of Amyotrophic Lateral Sclerosis in an Acromegalic Patient After Surgical Resection[doi.org]

  • Progressive Bulbar Palsy

    A 12-month-old boy with progressive cranial nerve palsies followed by ventilatory failure demanding artificial ventilation, generalized muscle weakness, and rapid progression[ncbi.nlm.nih.gov] Symptoms include pharyngeal muscle weakness (involved with swallowing), weak jaw and facial muscles, progressive loss of speech, and tongue muscle atrophy.[secure.ssa.gov] Symptoms include pharyngeal muscle weakness (muscles that are involved in swallowing), weak facial muscles, progressive loss of speech, and tongue muscle atrophy.[advancedpsy.com]

  • Spinal Muscular Atrophy with Respiratory Distress Type 1

    This finding suggests the rapid progression of peripheral axonal neuropathy in SMARD1 that leads to its characteristic clinical course of respiratory failure and paralysis[ncbi.nlm.nih.gov] Spinal muscular atrophy is characterised by slowly progressive muscle weakness and atrophy of the limb muscles associated with motor neurone loss in the spinal cord.[patient.info] Over a period of one month, the infant showed rapid progression of distal muscular weakness with hand and foot contractures, which were suggestive of neuromuscular disease[ncbi.nlm.nih.gov]

  • Muscular Dystrophy

    This type usually occurs in the first to third decades of life and involves: the proximal (back of the body) muscles of the pelvis and shoulders slow to fairly rapid progressive[betterhealth.vic.gov.au] Abstract Facioscapulohumeral muscular dystrophy is an autosomal-dominant, slowly progressive myopathy that involves facial, shoulder, and upper arm muscles.[ncbi.nlm.nih.gov] The most common type of muscular dystrophy causes rapid muscle wasting and progressive weakness early in life, usually between the ages of 2 and 5.[stanfordhealthcare.org]

  • Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2Q

    One family has shown rapid progression of the disorder in adolescence (summary by Gundesli et al., 2010).[ncbi.nlm.nih.gov] There is often asymmetric quadriceps, hamstring, biceps, brachioradialis, or calf weakness and atrophy. Muscle pain is common.[emedicine.medscape.com] DMD is the most severe form of muscular dystrophy and it is characterized as follows1: Rapid progression of muscle weakness, often with calf hypertrophy Decreased levels of[centogene.com]

  • Fazio-Londe Disease

    progression to death or later onset, less prominent respiratory symptoms and protracted clinical course.[ncbi.nlm.nih.gov] Symptoms include pharyngeal muscle weakness (involved with swallowing), weak jaw and facial muscles, progressive loss of speech, and tongue muscle atrophy.[secure.ssa.gov] progression to death or later onset, less prominent respiratory symptoms and lengthy clinical course.[diseaseinfosearch.org]

  • Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2T

    DMD is the most severe form of muscular dystrophy and it is characterized as follows1: Rapid progression of muscle weakness, often with calf hypertrophy Decreased levels of[centogene.com] Specifically, LGMD2B is a slowly progressive disease that causes muscle weakness and wasting ( atrophy ) of the pelvic muscles and muscles of the shoulder girdle. 0003236[rarediseases.info.nih.gov] The more common LGMD2 generally has an earlier age of onset, worse symptoms and more rapid progression compared to LGMD1.[chs-journal.com]

  • Motor Neuron Disease

    Both cases showed rapid progression to mutism within a few years. Neuropathologically, frontal lobe degeneration including the precentral gyrus was observed.[ncbi.nlm.nih.gov] Symptoms include pharyngeal muscle weakness (involved with swallowing), weak jaw and facial muscles, progressive loss of speech, and tongue muscle atrophy.[web.archive.org] Usually the onset is gradual but younger patients may show a more rapid progression.[southerncross.co.nz]

  • Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2J

    DMD is the most severe form of muscular dystrophy and it is characterized as follows1: Rapid progression of muscle weakness, often with calf hypertrophy Decreased levels of[centogene.com] Specifically, LGMD2B is a slowly progressive disease that causes muscle weakness and wasting ( atrophy ) of the pelvic muscles and muscles of the shoulder girdle. 0003236[rarediseases.info.nih.gov] The more common LGMD2 generally has an earlier age of onset, worse symptoms and more rapid progression compared to LGMD1.[chs-journal.com]

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