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خرید پکیج
تعداد آیتم قابل مشاهده باقیمانده : 3 مورد
نسخه الکترونیک
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Clinical findings in inherited fibrinogen disorders

Clinical findings in inherited fibrinogen disorders
  Bleeding complications Thromboembolic complications Complications of pregnancy Other findings (rare)
Afibrinogenemia
  • Common
  • Can be severe
  • Can occur during neonatal period (eg, umbilical cord bleeding)
  • Sites may include gastrointestinal, urinary, central nervous system, spleen (with splenic rupture)
  • Possible
  • May be venous or arterial
  • Spontaneous abortion, early fetal loss, and/or placental abruption may occur
  • Can have bleeding antepartum or postpartum
  • Bone cysts
  • Abnormal wound healing
Hypofibrinogenemia
  • Variable frequency
  • Variable severity
  • Rare but possible
  • May be venous or arterial
  • Spontaneous abortion may occur; the likelihood of successful pregnancy appears to correlate with the fibrinogen level
  • Can have bleeding antepartum or postpartum
  • Hepatic storage disease
Dysfibrinogenemia and hypodysfibrinogenemia
  • Variable frequency; affects less than half of individuals
  • Most bleeding is mild, but severe bleeding can occur
  • Common sites include menorrhagia and skin bleeding
  • More common than bleeding; may affect up to 30% of individuals
  • May occur in the setting of fibrinogen replacement therapy
  • Spontaneous abortion and postpartum hemorrhage may occur
  • Renal amyloidosis secondary to mutant fibrinogen (alpha-chain)
Refer to UpToDate for additional details regarding the clinical manifestations and evaluation of fibrinogen disorders.
Graphic 114456 Version 1.0

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