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Disease: Acrogeria- gottron type

  • A novel in-frame deletion in ZMPSTE24 is associated with autosomal recessive acrogeria (Gottron type) in an extended consanguineous family
  • A rare case of acrogeria, Gottron type with borderline personality disorder
  • Acrogeria (Gottron type): a vascular disorder?
  • Acrogeria of the Gottron type in a mother and son
  • Case of acrogeria of Gottron; place of acrogeria among various types of congenital skin atrophy
  • COL3A1 mutation leading to acrogeria (Gottron Type)
  • Ehlers-Danlos type IV syndrome presenting as renovascular hypertension
  • Grotton's acrogeria with bone involvement
  • Management of patient with acrometageria for routine dental treatment: A case report
  • Sudden death in acrogeria Gottron type
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CheckOrphan is a non-profit organization located in Basel, Switzerland and Santa Cruz, California that is dedicated to rare, orphan and neglected diseases. CheckOrphan offers users an interactive and dynamic platform for all these diseases. This strategy allows visitors to be updated daily on all the latest news and interact with people internationally. This is essential, because due to the nature of these diseases, there is not a large concentration of individuals within any given proximity.
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