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6,281 Possible Causes for Bilateral Pelvic Girdle 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

    Symptoms - Muscular dystrophy limb girdle type 2A- Erb type Muscle weakness is first evident in the shoulder girdle and later in the pelvic girdle.[checkorphan.org] 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]

  • Becker Muscular Dystrophy

    Little is known about parental motivations and expectations for clinical trials for rare pediatric disorders.[ncbi.nlm.nih.gov] 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[webmd.com] Breath stacking in children with neuromuscular disorders. Pediatr Pulmonol . 2013 Aug 16. [Medline] .[emedicine.medscape.com]

  • Poliomyelitis

    Post-polio syndrome (PPS) develops in approximately 30% of polio survivors several decades after the acute attack of paralytic poliomyelitis. Some of these patients develop post-poliomyelitis muscular atrophy (PPMA) which is characterized by a slowly progressive muscle weakness. Due to its clinicopathological[…][ncbi.nlm.nih.gov]

    Missing: Clumsy Gait
  • Hereditary Areflexic Dystasia

    National Organization for Rare Disorders (NORD). 2004; . Kleigman. Chapter 612 - Hereditary Motor-Sensory Neuropathies. Nelson Textbook of Pediatrics, 18th edition.[rarediseases.info.nih.gov] 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[jamanetwork.com] They noticed that prominent features of this disorder were an unsteady gait during early childhood and areflexia, or the absence of reflexes, which eventually led to clumsiness[en.wikipedia.org]

    Missing: Bilateral Pelvic Girdle Weakness
  • Hallervorden-Spatz Syndrome

    […] treatments and interventions Covers neurological, neuropsychiatric, and neuromedical disorders across the lifespan (pediatric, adult, and geriatric populations) Includes[books.google.com] Clumsiness, gait disturbance, and difficulty with tasks requiring fine motor coordination are common presenting symptoms. Motor tics are often seen.[disorders.eyes.arizona.edu] , gait (walking) problems, difficulty controlling movement, and speech problems.[rarediseases.org]

    Missing: Bilateral Pelvic Girdle Weakness
  • Niemann-Pick Disease

    Unit, Department of Pediatrics, Verona, Italy.[ncbi.nlm.nih.gov] , clumsiness, problems in walking (ataxia) Difficulty in posturing of limbs (dystonia) Slurred, irregular speech (dysarthria) Learning difficulties and progressive intellectual[npuk.org] Symptoms may include: Difficulty moving limbs that may lead to unsteady gait, clumsiness, walking problems Enlarged spleen Enlarged liver Jaundice at (or shortly after) birth[medlineplus.gov]

    Missing: Bilateral Pelvic Girdle Weakness
  • Metachromatic Leukodystrophy

    Neurology , Center for Childhood White Matter Disorders, VU University Medical Center , Amsterdam , The Netherlands 2 Amsterdam Neuroscience , VU University Medical Center[jnnp.bmj.com] Clumsiness, gait problems, slurred speech, incontinence, bizarre behavior and seizures are also observed.[genedx.com] In early-onset juvenile MLD, symptoms such as clumsiness and gait problems may be noticed first.[thinkgenetic.com]

    Missing: Bilateral Pelvic Girdle Weakness
  • Pyridoxine Dependency Syndrome

    The pediatric neurotransmitter disorders. J Child Neurol. 2007 May;22(5):606-16. Review.[ghr.nlm.nih.gov] […] and numb feet to numbness and clumsiness of hands.[drugs.com] Pediatr Neurol. 2006; 34 :164–7. [ PubMed : 16458834 ] Ohtsuka Y, Hattori J, Ishida T, Ogino T, Oka E.[ncbi.nlm.nih.gov]

    Missing: Bilateral Pelvic Girdle Weakness
  • 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.[oatext.com] Ataxic Gait Most commonly seen in cerebellar disease, this gait is described as clumsy, staggering movements with a wide-based gait.[web.archive.org] Clinical Pediatric Neurology, 6th Edition, by Gerald M.[books.google.com]

    Missing: Bilateral Pelvic Girdle Weakness