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263 Possible Causes for Diffuse Osseous Demineralization, Unstable Gait

  • Lyme Disease

    osseous structures.[doi.org] The one patient in the doxycycline group who reported severe arthralgia at the last follow-up had a history of multiple dorsal and lumbar fractures with diffusely demineralized[doi.org]

  • Lyme Neuroborreliosis

    osseous structures.[doi.org] The one patient in the doxycycline group who reported severe arthralgia at the last follow-up had a history of multiple dorsal and lumbar fractures with diffusely demineralized[doi.org]

  • Non-Hodgkin Lymphoma

    Non-Hodgkin lymphoma (NHL) is a group of blood cancers that includes all types of lymphoma except Hodgkin's lymphomas. Symptoms include enlarged lymph nodes, fever, night sweats, weight loss and tiredness. Other symptoms may include bone pain, chest pain or itchiness. Some forms are slow-growing, while others are[…][en.wikipedia.org]

    Missing: Diffuse Osseous Demineralization
  • Susac Syndrome

    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]

    Missing: Diffuse Osseous Demineralization
  • 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: Diffuse Osseous Demineralization
  • Autosomal Recessive 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: Diffuse Osseous Demineralization
  • Huntington Disease-Like 1

    Homepage Rare diseases Search Search for a rare disease Huntington disease-like 1 Disease definition A rare, genetic, human prion disease characterized by adult-onset neurodegenertaive manifestations associated with a movement disorder and psychiatric/behavioral disturbances. Patients typically present personality[…][orpha.net]

    Missing: Diffuse Osseous Demineralization
  • Huntington Disease-Like 3

    Charles David Marsden was Professor of Neurology at the Institute of Neurology/Neurosurgery at Queen Square and a leading figure in the study of Movement Disorders. Among his many significant scientific contributions were the pioneering of evoked responses, and transcranial electrical and magnetic stimulation as[…][books.google.com]

    Missing: Diffuse Osseous Demineralization
  • 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: Diffuse Osseous Demineralization
  • 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: Diffuse Osseous Demineralization

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