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33 Possible Causes for Bilateral Arm Weakness, Clumsy Gait, Pediatric Disorder

  • Duchenne Muscular Dystrophy

    BACKGROUND AND PURPOSE: Duchenne muscular dystrophy (DMD) is a lethal progressive pediatric muscle disorder and genetically inherited as an X-linked disease that caused by[ncbi.nlm.nih.gov] Additional early signs and symptoms include: Developmental delay Muscle weakness Clumsiness Waddling gait Difficulty or inability to perform activities such as climbing stairs[pfizer.com] Nelson Textbook of Pediatrics. 17th ed. Philadelphia, PA: Elsevier Saunders; 2005:2060-9. Acsadi G. Duchenne Muscular Dystrophy. NORD Guide to Rare Disorders.[rarediseases.org]

  • Erb Muscular Dystrophy

    Other neuromuscular disorders. Weinstein SL, Flynn JM, eds. Lovell and Winter's Pediatric Orthopaedics. 7th ed.[emedicine.medscape.com] Physical Exam Symptoms progressive weakness affecting proximal muscles first (begins with gluteal muscle weakness) gait abnormalities delayed walking toe walking clumsy, waddling[orthobullets.com] Other neuromuscular disorders. Weinstein SL, Flynn JM, eds. Lovell and Winter's Pediatric Orthopaedics . 7th ed.[emedicine.medscape.com]

  • Glycogen Storage Disease Type 2

    Nomenclature for Conditions based upon “Naming and Counting Disorders (Conditions) Included in Newborn Screening Panels.” Pediatrics. 2006; 117 (5) Suppl: S308-S314.[hrsa.gov] Patients with the latter two types may manifest with primarily neurologic symptoms of clumsiness, gait disturbance, worsening of coordination, and fine motor skills, or with[dx.doi.org] Dowling, Myopathies and Myotonic Disorders, Pediatric Electromyography, 10.1007/978-3-319-61361-1_22, (327-354), (2017). G. Chalès and P.[dx.doi.org]

  • Friedreich Ataxia

    Torso and arms Action and intention tremors Choreiform movements Associated impaired proprioception, vibration sense ( pallhypesthesia ), and loss of deep tendon reflexes[amboss.com] Leigh syndrome (subacute necrotizing encephalomyopathy) is a rare, highly morbid and fatal pediatric disorder that results in severe neurological and neuromuscular dysfunction[bioelectron.com] General clumsiness and gait ataxia are usually the first signs to appear, often followed by pyramidal signs, upper-limb ataxia and dysarthria.[orpha.net]

  • Wilson Disease

    The abductor pollicis brevis, first dorsal interosseous, other intrinsic hand muscles, and toe and feet muscles were weak (Medical Research Council [MRC] grade IV /IV ) bilaterally[jamanetwork.com] disorders Genotype–phenotype correlation Summary Chapter 13: Other organ involvement and clinical aspects of Wilson disease Karolina Dziezyc, Tomasz Litwin and Anna Czlonkowska[elsevier.com] Tremors, involuntary muscle movements, clumsy gait and speech difficulties usually improve with treatment for Wilson's disease.[mayoclinic.org]

  • Platybasia

    Links Abstract Hadju—Cheney syndrome (HCS) is a rare autosomal-dominant disorder with variable expressivity.[thejns.org] The symptoms may also include clumsiness, numbness along one side of the body, unsteadiness of the gait, vertigo, weakness of one side of the body, loss of control of bowel[xpertdox.com] Although CM-I occurs in both pediatric and adult patients, its prevalence, clinical features and management in the pediatric population are not well defined.[science.gov]

  • Binswanger Disease

    weakness of distal proximal muscles in the arm leg, bladder dysfunction, and a variable degree of sensory loss below the level of injury central herniation downward displacement[strokecenter.org] […] treatments and interventions Covers neurological, neuropsychiatric, and neuromedical disorders across the lifespan (pediatric, adult, and geriatric populations) Includes[books.google.de] Other symptoms include forgetfulness (but not as severe as the forgetfulness of Alzheimer's disease), changes in speech, an unsteady gait, clumsiness or frequent falls, changes[ninds.nih.gov]

  • Transient Ischemic Attack

    A 69-year-old gentleman presented with a TIA episode (dysarthria, right-arm weakness, and numbness).[ncbi.nlm.nih.gov] […] stroke. 651 – 653 The most prevalent inherited coagulation disorder is factor V Leiden, which is resistant to neutralization by activated protein C. 654 In a meta-analysis[doi.org] Coordination Clumsy arms, legs, or trunk; loss of balance or falling (particularly to one side) with standing or walking Incoordination of limbs, trunk, or gait may indicate[aafp.org]

  • Hemiparesis

    This article specifically focuses on the neurological symptoms that manifest because of these disorders and their treatments.[ncbi.nlm.nih.gov] Ataxic Gait Most commonly seen in cerebellar disease, this gait is described as clumsy, staggering movements with a wide-based gait.[stanford25.wordpress.com] Abstract There is a growing interest in the extraintestinal manifestations of common pediatric gastrointestinal diseases, such as inflammatory bowel disease and celiac disease[ncbi.nlm.nih.gov]

  • Upper Limb Hypertrophy

    […] as late effects of cerebrovascular accident Weakness of arm Weakness of bilat arms Weakness of bilat legs Weakness of bilateral legs Weakness of both arms Weakness of extremities[icd9data.com] Pediatric Hand and Upper Limb Surgery guides you to the present indications for intervention and care in upper limb pediatric disorders.[books.google.com] Suspicion of joint or muscle disease (e.g., pain, swelling, stiffness, clumsiness, weakness; this may be suggested if toe-walking is new and a change from a previous gait[pmmonline.org]