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266 Possible Causes for Onset of Encephalopathy between Ages 2 and 3 Years, Unstable Gait

  • Susac Syndrome

    Susac syndrome is more common in women, with ratio of 3:1, the age of onset fluctuates between 9 and 58 years [2].[medwave.cl] His gait was unstable and he could not walk in tandem. His behavior was disinhibited and he expressed paranoid and delusional thoughts.[the-rheumatologist.org] Introduction Susac syndrome is a rare disorder, initially described by John Susac in 1979, who reported two female cases with the classical triad of subacute encephalopathy[medwave.cl]

  • Non-Hodgkin Lymphoma

    There are many different types of non-Hodgkin lymphoma (NHL). Doctors also give NHL a grade, depending on how quickly it is likely to grow. Low grade NHL Find out about low grade non-Hodgkin lymphoma (NHL), what low grade means, and different types. High grade NHL Find out about high grade lymphomas, what high[…][cancerresearchuk.org]

    Missing: Onset of Encephalopathy between Ages 2 and 3 Years
  • Lyme Neuroborreliosis

    Lyme neuroborreliosis (LNB) is a nervous system infection caused by Borrelia burgdorferi sensu lato (Bb). To present evidence-based recommendations for diagnosis and treatment. Data were analysed according to levels of evidence as suggested by EFNS. The following three criteria should be fulfilled for definite[…][ncbi.nlm.nih.gov]

    Missing: Onset of Encephalopathy between Ages 2 and 3 Years
  • Lyme Disease

    Abstract Lyme disease is the most common vector-borne disease in the United States. A number of other spirochetal diseases, if contracted in pregnancy, have been shown to cause fetal harm and there is concern over a similar effect with gestational borreliosis. Previously published individual case reports have[…][doi.org]

    Missing: Onset of Encephalopathy between Ages 2 and 3 Years
  • X-linked Distal Spinal Muscular Atrophy Type 3

    Homepage Rare diseases Search Search for a rare disease X-linked distal spinal muscular atrophy type 3 Disease definition X-linked distal spinal muscular atrophy type 3 is a rare distal hereditary motor neuropathy characterized by slowly progressive atrophy and weakness of distal muscles of hands and feet with[…][orpha.net]

    Missing: Onset of Encephalopathy between Ages 2 and 3 Years
  • Limb-Girdle Muscular Dystrophy Type 2C

    BACKGROUND: Limb-girdle muscular dystrophy type 2C (LGMD2C) is an autosomal recessive muscle dystrophy that resembles Duchenne muscular dystrophy (DMD). Although DMD is known to affect one in every 3500 males regardless of race, a widespread founder mutation causing LGMD2C has been described in North Africa.[…][ncbi.nlm.nih.gov]

    Missing: Onset of Encephalopathy between Ages 2 and 3 Years
  • Huntington Disease-Like 1

    April 18, 2017 ; 88 (16 Supplement) April 24, 2017 Victor Calil da Silveira , Luiz Felipe Vasconcellos , Mariana Spitz , Vitor Tumas First published April 17, 2017, Abstract Objective: This study aims to report a series of six patients with genetic diagnosis of Huntington disease-like type 2 (HDL2) and to describe the[…][neurology.org]

    Missing: Onset of Encephalopathy between Ages 2 and 3 Years
  • Huntington Disease-Like 3

    WHO-ICD-10 version:2010 Diseases of the nervous system Systemic atrophies primarily affecting the central nervous system Mode of Inheritance Autosomal Recessive Gene Map Locus Huntington disease-like (HDL) syndromes are conditions that resemble Huntington disease, but are not caused by the same mutant[…][cags.org.ae]

    Missing: Onset of Encephalopathy between Ages 2 and 3 Years
  • Autosomal Recessive Spinocerebellar Ataxia Type 17

    Gait ataxia is characterized by unstable walk and standing, which slowly progresses with the appearance of some of the other symptoms, such as abnormal hand movements, involuntary[encyclopedia.com] SCA10 ataxia is caused by an unstable protein repeat on chromosome 22.[encyclopedia.com] Dystonia (spasticity or involuntary and repetitive movements) or gait ataxia is usually the initial symptom in children.[encyclopedia.com]

    Missing: Onset of Encephalopathy between Ages 2 and 3 Years
  • Autosomal Recessive Spinocerebellar Ataxia

    His gait became progressively unstable from childhood, and started to interfere with his daily activities after the age of 45.[jmg.bmj.com]

    Missing: Onset of Encephalopathy between Ages 2 and 3 Years

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