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70 Possible Causes for Late-Onset Thrombocytopenia

  • Thrombocytopenia

    Table 3 Comparison of natural history of early and late onset thrombocytopenia in neonates Late onset thrombocytopenia Our recent work 17 clearly shows that thrombocytopenia[doi.org] The most frequent causes for NT were early and late onset sepsis and asphyxia.[ncbi.nlm.nih.gov] This late onset thrombocytopenia has a distinct natural history (table 3).[doi.org]

  • Puerperium

    Late onset GBS disease (LOD) Late onset disease (LOD) occurs beyond seven days of life and can develop up to three months of age ( Yagupsky 1991 ).[doi.org] In the same study, all infants born at term survived, but the mortality rate for preterm neonates with early symptomatic disease (and who presented with shock and thrombocytopenia[doi.org]

  • Birth

    Late onset GBS disease (LOD) Late onset disease (LOD) occurs beyond seven days of life and can develop up to three months of age ( Yagupsky 1991 ).[doi.org] In the same study, all infants born at term survived, but the mortality rate for preterm neonates with early symptomatic disease (and who presented with shock and thrombocytopenia[doi.org]

  • Autoimmune Thrombocytopenia

    Physicians must be aware that autoimmune thrombocytopenia can occur even after the end of treatment, as a late onset complication, especially when using the pegylated forms[ncbi.nlm.nih.gov] Table 3 Comparison of natural history of early and late onset thrombocytopenia in neonates Late onset thrombocytopenia Our recent work 17 clearly shows that thrombocytopenia[fn.bmj.com] This late onset thrombocytopenia has a distinct natural history (table 3).[fn.bmj.com]

  • Thrombocytopenia Due to Sequestration

    The table below contrasts Early from Late Onset Thrombocytopenia: Early Onset ( 72 hours after birth) Late Onset ( 72 hours after birth) Degree of Thrombocytopenia Mild to[learn.pediatrics.ubc.ca] Neonatal Intensive Care Unit Patients It can be divided into Early Onset and Late Onset Thrombocytopenia.[learn.pediatrics.ubc.ca] onset thrombocytopenia in neonates.[learn.pediatrics.ubc.ca]

  • Unverricht-Lundborg Syndrome

    […] scapuloperoneal muscular dystrophy MYH7-related late-onset scapuloperoneal syndrome MYH7-related late-onset SPMD MYH9-RD MYH9-related disease MYH9-related disorder MYH9-related[orpha.net] […] of PDGFRA, PDGFRB or FGFR1 Myeloid sarcoma Myelomatosis Myelomeningocele Myeloperoxidase deficiency Myeloproliferative disorder Myeloproliferative neoplasm MYH7-related late-onset[orpha.net] […] syndrome MYH9-related syndromic thrombocytopenia Myhre-Riley-Smith syndrome Myhre syndrome Myiasis MYO5B deficiency MYO5B-related progressive familial intrahepatic cholestasis[orpha.net]

  • Benign Adult Familial Myoclonic Epilepsy

    […] scapuloperoneal muscular dystrophy MYH7-related late-onset scapuloperoneal syndrome MYH7-related late-onset SPMD MYH9-RD MYH9-related disease MYH9-related disorder MYH9-related[orpha.net] […] of PDGFRA, PDGFRB or FGFR1 Myeloid sarcoma Myelomatosis Myelomeningocele Myeloperoxidase deficiency Myeloproliferative disorder Myeloproliferative neoplasm MYH7-related late-onset[orpha.net] […] syndrome MYH9-related syndromic thrombocytopenia Myhre-Riley-Smith syndrome Myhre syndrome Myiasis MYO5B deficiency MYO5B-related progressive familial intrahepatic cholestasis[orpha.net]

  • Plasmablastic Lymphoma

    Delayed and late onset forms have a wide spectrum of manifestations mostly involving immunological and autoimmune system (i.e., hemolytic anemia and immune thrombocytopenia[frontiersin.org]

  • Drug-induced Thrombocytopenia

    […] of complex therapies (rifampicin and abciximab causing late onset thrombocytopenia).[ncbi.nlm.nih.gov] We describe two cases of isolated thrombocytopenia in which cytometric analysis, a readily available technique, allowed the identification of the causative drug in the context[ncbi.nlm.nih.gov]

  • Microangiopathy

    Effective strategies are needed for late-onset TMA after LDLT to improve treatment response and survival.[cjasn.asnjournals.org] Thrombotic microangiopathy (TMA) includes syndromes of microangiopathic hemolytic anemia, thrombocytopenia, renal dysfunction, fever, neurologic deficits, and associated organ[cjasn.asnjournals.org]

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