Create issue ticket

302 Possible Causes for Cardiomyopathy, Clumsy Gait, Pediatric Disorder

  • Duchenne Muscular Dystrophy

    She was treated for peripartum cardiomyopathy (PPCM) with angiotensin converting enzyme inhibitors (ACEi), beta-blockers and diuretics with normalisation of her cardiac function[ncbi.nlm.nih.gov] 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]

  • Friedreich Ataxia

    They may develop a cardiomyopathy (CM) phenotype, which is similar to hypertrophic cardiomyopathy and potentially progresses towards a life-limiting problem.[escardio.org] 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]

  • Glycogen Storage Disease Type 2

    , lysosomal disease with hypertrophic cardiomyopathy, glycogen storage disease with hypertrophic cardiomyopathy, lysosomal glycogen storage disease Prende il nome da Johannes[commons.wikimedia.org] 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]

  • Mucopolysaccharidosis 2

    Diarrhea Short stature Skeletal deformities Joint stiffness Inguinal or umbilical hernia Developmental delay Intellectual disability Hyperactivity Seizures Hepatomegaly Cardiomyopathy[symptoma.com] Abstract Mucopolysaccharidosis type II (MPSII) is an inherited disorder due to a deficiency of the lysosomal enzyme iduronate-2-sulfatase (IDS).[ncbi.nlm.nih.gov] Gait was noted to be clumsy and stiff. Range of motion in all extremities was limited, and the arms and legs were slightly flexed.[amhsr.org]

  • Becker Muscular Dystrophy

    Patients with Becker muscular dystrophy-related cardiomyopathy typically survive into their 30s, when they succumb to complications of cardiomyopathy or receive heart transplants[ncbi.nlm.nih.gov] 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]

  • Wilson Disease

    Cardiac injury may include arrhythmia, cardiomyopathy, and autonomic dysfunction.[ncbi.nlm.nih.gov] 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]

  • Erb Muscular Dystrophy

    […] insufficiency MedLine Citation: PMID: 6706057 Owner: NLM Status: MEDLINE Abstract/OtherAbstract: We describe a case of Erb's limb girdle muscular dystrophy with congestive cardiomyopathy[biomedsearch.com] 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]

  • Beriberi

    In both diseases, cardiac involvement may occur as dilated cardiomyopathy.[ncbi.nlm.nih.gov] A 71 year-old man with a history of partial gastrectomy presented to the emergency department with subacute gait instability associated with painful dysesthesias and clumsiness[dx.doi.org] They are Shoshin beriberi, beriberi with high output failure, beriberi with signs of a hyperdynamic circulation alone and beriberi with underlying cardiomyopathy.[ncbi.nlm.nih.gov]

  • Hereditary Areflexic Dystasia

    Lascelles , RG , Baker , IA and Thomas , PK ( 1970 ) Hereditary polyneuropathy of Roussy-Levy type with associated cardiomyopathy . Guy Hosp Rep 119 : 253 – 262 .[cambridge.org] 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]

  • Muscular Dystrophy

    A pilot study was conducted to assess the safety and efficacy of tranilast in muscular dystrophy patients with cardiomyopathy.[ncbi.nlm.nih.gov] We offer children and families coordinated care for the diagnosis and treatment of muscular dystrophy and other pediatric neuromuscular disorders.[ynhh.org] Other symptoms include loss of some reflexes, a waddling gait, frequent falls and clumsiness (especially when running), difficulty when rising from a sitting or lying position[web.archive.org]

Similar symptoms