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17 Possible Causes for Dementia (Onset in Fifth Decade)

Did you mean: Dementia (Onset in Fifth Decade

  • Alzheimer Disease

    […] in the fourth decade of life, usually leading to death in the fifth decade of life. 42-44 Loss-of-function mutations in DAP12 and TREM2 were originally found in patients[doi.org] […] in the fourth decade of life, usually leading to death in the fifth decade of life. 42 – 44 Loss-of-function mutations in DAP12 and TREM2 were originally found in patients[ncbi.nlm.nih.gov] It is a rare recessively inherited disease that is characterized by painful bone cysts in wrists and ankles, psychotic symptoms, and progressive presenile dementia with onset[doi.org]

  • Autosomal Dominant Prognathism

    (onset in fifth decade); Choreiform movements; Gait abnormalities (less common); Atrophy of hippocampal dentate gyrus; Alpha-B-crystallin expression in oligodendrocytes;[findzebra.com] […] dominant HEAD AND NECK: [Eyes]; Congenital cataracts; Blindness; Nystagmus ABDOMEN: [Gastrointestinal]; Dysphagia NEUROLOGIC: [Central nervous system]; Intellectual impairment; Dementia[findzebra.com]

  • Olivopontocerebellar Atrophy

    The familial form has an earlier onset (second decade) and may feature spinal cord atrophy.[ucl.ac.uk] Additional clinical features may include MUSCLE RIGIDITY; NYSTAGMUS, PATHOLOGIC; RETINAL DEGENERATION; MUSCLE SPASTICITY; DEMENTIA; URINARY INCONTINENCE; and OPHTHALMOPLEGIA[profiles.umassmed.edu] The sporadic form tends to present in the fifth or sixth decade, and is considered a clinical subtype of MULTIPLE SYSTEM ATROPHY.[ucl.ac.uk]

  • Juvenile Huntington Disease

    A familial disorder inherited as an autosomal dominant trait and characterized by the onset of progressive CHOREA and DEMENTIA in the fourth or fifth decade of life.[ebi.ac.uk] […] and fifth decades.[e-jmd.org] […] the fourth or fifth decade of life.[ebi.ac.uk]

  • Huntington's Disease

    […] of progressive chorea and dementia in the fourth or fifth decade of life.[icd9data.com] […] from huntingtons chorea Huntingtons chorea Progressive chorea Clinical Information A familial disorder inherited as an autosomal dominant trait and characterized by the onset[icd9data.com] […] due to Huntington chorea Dementia due to Huntington chorea with altered behavior Dementia due to Huntingtons chorea w behavior changes Dementia due to Huntingtons disease Dementia[icd9data.com]

  • Huntington Disease-Like 2

    […] of progressive chorea and dementia in the fourth or fifth decade of life.[icd10data.com] […] from huntingtons chorea Huntington's chorea Huntingtons chorea Clinical Information A familial disorder inherited as an autosomal dominant trait and characterized by the onset[icd10data.com] […] huntington chorea Dementia due to huntington chorea with altered behavior Dementia due to huntingtons disease Dementia due to huntingtons disease w behavioral disturbance Dementia[icd10data.com]

  • Adult Polyglucosan Body Disease

    […] within the fifth to seventh decade (88%), peripheral neuropathy (80%), dementia (64%), neurogenic bladder (72%), and upper motor neuron sign (80%), although most patients[synapse.koreamed.org] Its most consistent features are onset in the fifth to seventh decades (88%), peripheral neuropathy (80%), dementia (64%), neurogenic bladder (72%), and upper motor neuron[jnnp.bmj.com] […] progressive sensorimotor or pure motor peripheral neuropathy, upper motor neuron symptoms, neurogenic bladder, and cognitive impairment. 1 - 6 Its most consistent features are onset[synapse.koreamed.org]

  • Leukodystrophy

    The adult form has its onset in the fourth or fifth decades and is marked mainly by cerebellar, autonomic, and pyramidal disorders.[icd9data.com] The early symptoms include rotary movements of the head and eyes, which may vanish later in life, usually followed by spasticity of the legs and arms, cerebellar ataxia, dementia[icd9data.com]

  • Hereditary Sensory Neuropathy

    Onset of dementia occurred between the second and fourth decades of life and death occurred in the fifth and sixth decades of life.[hsan1esociety.org] Hereditary sensory neuropaihy type 1E (HSN1E, OMIM 614116) was first described in a multi-generation American family with adult-onset distal sensory impairment and subsequent[hsan1esociety.org]

  • Pelizaeus-Merzbacher Disease

    The adult form has its onset in the fourth or fifth decades and is marked mainly by cerebellar, autonomic, and pyramidal disorders.[icd9data.com] The early symptoms include rotary movements of the head and eyes, which may vanish later in life, usually followed by spasticity of the legs and arms, cerebellar ataxia, dementia[icd9data.com]

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