Latent Autoimmune Diabetes in Stiff-Person Syndrome: Table 1
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چکیده
منابع مشابه
Latent autoimmune diabetes in Stiff-Person Syndrome.
GAD antibody (GADA) positivity is a hallmark of autoimmune diabetes and the rare autoimmune neurological disorder Stiff-Person Syndrome (SPS). Concomitant SPS and classical type 1 diabetes (T1D) have been described in case reports (1–3). A recent series of SPS reported the prevalence of T1D at 43% (4). However, the presence of alternative forms of autoimmune diabetes, such as latent autoimmune ...
متن کاملRhabdomyolysis and Autoimmune Variant Stiff-Person Syndrome
Stiff-person syndrome (SPS) is a rare neurologic disorder characterized by waxing and waning muscular rigidity, stiffness and spasms. Three subtypes have been described: paraneoplastic, autoimmune and idiopathic. Rhabdomyolysis has been described in the paraneoplastic variant, but to our knowledge no case has been reported involving the autoimmune variant. We report a case report of a 50-year-o...
متن کاملStiff eyes in stiff-person syndrome.
since 1951, it is now a weekly with 48 issues per year.
متن کاملRigidity and spasms from autoimmune encephalomyelopathies: stiff-person syndrome.
Stiff-person syndrome (SPS) is a disorder characterized by progressive muscle rigidity with superimposed painful muscle spasms and gait impairment due to continuous motor activity. Evidence has accumulated in favor of SPS representing an autoimmune, predominantly encephalomyelopathic disorder resulting from B-cell-mediated clonal production of autoantibodies against presynaptic inhibitory epito...
متن کاملStiff Person Syndrome.
Stiff-person syndrome or Moersch-Woltmann is a very rare and disabling neurologic disorder characterized by muscle rigidity and episodic spasms involving axial and limb musculature. It is an autoimmune disorder resulting in a malfunction of aminobutyric acid mediated inhibitory networks in the central nervous system. We describe a patient of stiff person syndrome.
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ژورنال
عنوان ژورنال: Diabetes Care
سال: 2014
ISSN: 0149-5992,1935-5548
DOI: 10.2337/dc14-1444