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117 Possible Causes for Facial Muscle Weakness and Progressive Atrophy, Muscle Weakness

  • Muscular Dystrophy

    It causes progressive weakness in muscles of the face, arms, legs, and around the shoulders and chest.[ninds.nih.gov] Abstract Facioscapulohumeral muscular dystrophy is an autosomal-dominant, slowly progressive myopathy that involves facial, shoulder, and upper arm muscles.[ncbi.nlm.nih.gov] Occasionally, however, females who carry a DMD gene mutation may have muscle weakness and cramping.[web.archive.org]

  • Motor Neuron Disease

    Onset was in the second to fourth decade with finger extension weakness, progressing to other distal and sometimes more proximal muscles.[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] Progressive bulbar palsy , also called progressive bulbar atrophy, involves the brain stem—the bulb-shaped region containing lower motor neurons needed for swallowing, speaking[ninds.nih.gov]

  • Multifocal Motor Neuropathy

    Her disease was difficult to manage with various immunosuppressants, and the muscle weakness eventually progressed to involve the respiratory muscles, necessitating mechanical[ncbi.nlm.nih.gov] In the first patient the symptoms were slowly progressive with bulbar muscle impairment, generalized weakness, muscular atrophy with cramps and fasciculations.[moh-it.pure.elsevier.com] Most patients showed not only muscle weakness but also fatigue, limited dexterity, and limited walking ability.[ncbi.nlm.nih.gov]

  • Facioscapulohumeral Muscular Dystrophy

    BACKGROUND: Although muscle weakness is a hallmark of facioscapulohumeral muscular dystrophy (FSHD), the molecular mechanisms that lead to weakness in FSHD remain largely[ncbi.nlm.nih.gov] Facioscapulohumeral muscular dystrophy is an autosomal-dominant, slowly progressive myopathy that involves facial, shoulder, and upper arm muscles.[ncbi.nlm.nih.gov] FSHD affects about one in 20-400,000 people, and no effective therapeutic strategies are known to halt disease progression or reverse muscle weakness or atrophy.[ncbi.nlm.nih.gov]

  • Inclusion Body Myositis

    We have identified several patients with sIBM in our cohort with muscle weakness of the flexors but not the quadriceps femoris.[ncbi.nlm.nih.gov] […] disease of middle-aged , beginning in legs, causing atrophy and weakness of quadriceps, sparing facial and oropharyngeal muscles EMG Abnormal electrical 'irritation', slowing[medical-dictionary.thefreedictionary.com] The most common symptoms were muscle weakness, falls, dysphagia, and weight loss. Hypertension was the main comorbidity.[ncbi.nlm.nih.gov]

  • Spinal Muscular Atrophy

    We report the case of a male who presented in infancy with motor delay and muscle weakness.[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] She presented with progressive muscle weakness, tremor, seizure, and cognitive impairment.[ncbi.nlm.nih.gov]

  • Adult Spinal Muscular Atrophy

    Muscle weakness seen in SMA4 is similar to the muscle weakness seen in other genetic conditions.[resourcerepository.org] 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] weakness and atrophy.[uniprot.org]

  • Spinal Muscular Atrophy Type 3

    Swallowing muscle weakness : Infants with swallowing or sucking weakness can be fed with a gastrostomy tube.[curascriptsd.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] SMA type 3 causes variable muscle weakness, cramps and fatigue.[rch.org.au]

  • Spinal Muscular Atrophy Type 1

    AIM: This study described end-of-life care for children affected by spinal muscular atrophy type 1 (SMA1), which is characterised by progressive muscle weakness and develops[ncbi.nlm.nih.gov] We present a baby with spinal muscular atrophy type 1, an inherited disorder causing progressive weakness, leading to complete paralysis of respiratory, facial and limb muscles[ncbi.nlm.nih.gov] BACKGROUND: Spinal muscular atrophy (SMA) is a neuromuscular disorder mainly characterized by proximal muscle weakness.[ncbi.nlm.nih.gov]

  • Progressive Muscular Atrophy

    She developed muscle weakness of the distal part of the left lower extremity at age 42, followed by muscle weakness and atrophy of the right lower extremity and upper extremities[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] She developed muscle weakness in the distal part of the right upper extremity at age 52, followed by muscle weakness in the left upper extremity and lower extremities at age[ncbi.nlm.nih.gov]

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