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113 Possible Causes for Clumsy Gait, Pediatric Disorder, Toe-Walking Gait

  • 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[] BMD can present in several ways: in children the first feature may be a toe walking gait or exercise-related cramps with or without myoglobinuria.[]

  • Hallervorden-Spatz Syndrome

    […] on toes and unsteady gait.[] […] treatments and interventions Covers neurological, neuropsychiatric, and neuromedical disorders across the lifespan (pediatric, adult, and geriatric populations) Includes[] Clumsiness, gait disturbance, and difficulty with tasks requiring fine motor coordination are common presenting symptoms. Motor tics are often seen.[]

  • Becker Muscular Dystrophy

    The gait is often affected leading to toe-walking gait. Due to this, they have a tendency to fall often.[] Little is known about parental motivations and expectations for clinical trials for rare pediatric disorders.[] Walking on the toes or balls of the feet Clumsiness, falling often Trouble climbing stairs Difficulty rising from a lying or sitting position Larger-than-normal calves that[]

  • Hereditary Areflexic Dystasia

    Usually, weakness begins in the feet and ankles, and manifests itself as foot drop — difficulty lifting the foot at the ankle, so that the toes point downward during walking[] National Organization for Rare Disorders (NORD). 2004; . Kleigman. Chapter 612 - Hereditary Motor-Sensory Neuropathies. Nelson Textbook of Pediatrics, 18th edition.[] IN 1926, Roussy and Lévy 1 described a familial syndrome characterized by (1) clumsy gait, (2) abnormalities of equilibrium which were evident on standing and more pronounced[]

  • Cerebral Palsy

    […] one foot or leg dragging; walking on the toes, a crouched gait, or a “scissored” gait; and muscle tone that is either too stiff or too floppy.[] Pediatric Nutrition Support Core Curriculum. Silver Spring, MD: A.S.P.E.N. Publishing; 2015:261. 45. Linscheid T. Behavioral treatments for pediatric feeding disorders.[] There is poor coordination, with a wide-based and clumsy gait. There is also difficulty with precise movements, such as using a pen or buttoning a shirt. Mixed.[]

  • Erb Muscular Dystrophy

    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.[] Other neuromuscular disorders. Weinstein SL, Flynn JM, eds. Lovell and Winter's Pediatric Orthopaedics . 7th ed.[]

  • Metachromatic Leukodystrophy

    The neurologic findings were consistent with mild spastic diplegia (occasionally with toe walking).[] Neurology , Center for Childhood White Matter Disorders, VU University Medical Center , Amsterdam , The Netherlands 2 Amsterdam Neuroscience , VU University Medical Center[] Clumsiness, gait problems, slurred speech, incontinence, bizarre behavior and seizures are also observed.[]

  • Infantile Hemiplegia

    [Crossref] Mak MK (2010) Reaching and grasping a moving target is impaired in children with developmental coordination disorder. Pediatr Phys Ther 22: 384-391.[] Ataxic Gait Most commonly seen in cerebellar disease, this gait is described as clumsy, staggering movements with a wide-based gait.[] Clinical Pediatric Neurology, 6th Edition, by Gerald M.[]

  • Rett Syndrome

    Shaky, unsteady, stiff gait or toe walking. Seizures. Slowing head growth beginning at 5 to 6 months of age. Loss of normal sleep patterns.[] El-Bitar, Degenerative Disorders Primarily of Gray Matter, Swaiman's Pediatric Neurology, 10.1016/B978-1-4377-0435-8.00041-X, (518-543), (2012). Eveline E. O.[] These mice do not express Mecp2 at all and they display the same symptoms as humans, such as normal development until about 6 weeks, regression, reduced movement, clumsy gait[]

  • Friedreich Ataxia

    The first symptom to appear is usually difficulty in walking, or gait Ataxia. The Ataxia gradually worsens and slowly spreads to the arms and then the trunk.[] 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.[]