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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[] Additional early signs and symptoms include: Developmental delay Muscle weakness Clumsiness Waddling gait Difficulty or inability to perform activities such as climbing stairs[] Nelson Textbook of Pediatrics. 17th ed. Philadelphia, PA: Elsevier Saunders; 2005:2060-9. Acsadi G. Duchenne Muscular Dystrophy. NORD Guide to Rare Disorders.[]

  • Erb Muscular Dystrophy

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

  • 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.[] 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[] Dowling, Myopathies and Myotonic Disorders, Pediatric Electromyography, 10.1007/978-3-319-61361-1_22, (327-354), (2017). G. Chalès and P.[]

  • Friedreich Ataxia

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

  • 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[] disorders Genotype–phenotype correlation Summary Chapter 13: Other organ involvement and clinical aspects of Wilson disease Karolina Dziezyc, Tomasz Litwin and Anna Czlonkowska[] Tremors, involuntary muscle movements, clumsy gait and speech difficulties usually improve with treatment for Wilson's disease.[]

  • Platybasia

    Links Abstract Hadju—Cheney syndrome (HCS) is a rare autosomal-dominant disorder with variable expressivity.[] 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[] Although CM-I occurs in both pediatric and adult patients, its prevalence, clinical features and management in the pediatric population are not well defined.[]

  • 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[] […] treatments and interventions Covers neurological, neuropsychiatric, and neuromedical disorders across the lifespan (pediatric, adult, and geriatric populations) Includes[] 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[]

  • Transient Ischemic Attack

    A 69-year-old gentleman presented with a TIA episode (dysarthria, right-arm weakness, and numbness).[] […] 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[] 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[]

  • Hemiparesis

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

  • 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[] Pediatric Hand and Upper Limb Surgery guides you to the present indications for intervention and care in upper limb pediatric disorders.[] 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[]