Mechanism for Autoimmune Diseases X Chromosome Monosomy: A Common

نویسندگان

  • Eric Gershwin
  • Mauro Podda
  • Mitchell Watnik
  • Francesca R. Grati
  • Giuseppe Simoni
  • Pier Luigi Meroni
  • Bianca Marasini
  • Silvana Zeni
  • Pier Maria Battezzati
  • Massimo Zuin
  • Pietro Invernizzi
  • Monica Miozzo
  • Carlo Selmi
  • Luca Persani
  • Simona Lucchi
  • M. Eric Gershwin
چکیده

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منابع مشابه

X-chromosome inactivation and autoimmunity

We thank Dr Ozcelik for his careful reading of our review and his thoughtful letter. Dr Ozcelik raises the issue of nonequivalence of monosomy X frequency and X-chromosome inactivation pattern (XCIP). The first refers to the proportion of cells with a single X chromosome, wherein transcription occurs from the lone X chromosome. The second refers to the ratio of inactivated maternal to paternal ...

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X-chromosome inactivation and autoimmunity

We thank Dr Ozcelik for his careful reading of our review and his thoughtful letter. Dr Ozcelik raises the issue of nonequivalence of monosomy X frequency and X-chromosome inactivation pattern (XCIP). The first refers to the proportion of cells with a single X chromosome, wherein transcription occurs from the lone X chromosome. The second refers to the ratio of inactivated maternal to paternal ...

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Response: X-chromosome inactivation and autoimmunity

We thank Dr Ozcelik for his careful reading of our review and his thoughtful letter. Dr Ozcelik raises the issue of nonequivalence of monosomy X frequency and X-chromosome inactivation pattern (XCIP). The first refers to the proportion of cells with a single X chromosome, wherein transcription occurs from the lone X chromosome. The second refers to the ratio of inactivated maternal to paternal ...

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A Rare Association of Monosomy 18p Syndrome and Polyglandular Autoimmune Syndrome Type IIIA

We report a monosomy 18p syndrome in a male patient with polyglandular autoimmune syndrome (PAS) type IIIA. A 34-year-old mentally retarded diabetic male patient with short stature, wide earlaps, old-looking face, straight nasal bone, atrophic mouth, drooping cheeks, full teeth loss, and soft, weak and sparse white hair was admitted to the outpatient endocrinology clinic. Chromosome analysis of...

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Autoimmune polyglandular syndrome type 2 manifested as Hashimoto's thyroiditis and adrenocortical insufficiency, in Turner syndrome woman, with onset following introduction of treatment with recombinant human growth hormone.

Autoimmune polyglandular syndrome is a constellation of signs and symptoms of simultaneous insufficiencies of several endocrine glands. Autoimmune polyglandular syndrome type 2 (APS 2) may be diagnosed when the adrenocortical insufficiency is associated with an autoimmune thyroid disease (Hashimoto's thyroiditis or Graves' disease), and/or insulin-dependent diabetes mellitus. Turner syndrome is...

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تاریخ انتشار 2005