Congenital Thrombasthenia In Children Welfare Teaching Hospital: A Descriptive Study
Background: Thrombasthenia is an inherited genetic disorder affecting platelets, which is characterized by spontaneous muco-cutaneous bleeding and abnormally prolonged bleeding in response to injury or trauma. Objectives: The aim of this study was to assess the diagnosis and treatment of thrombasthenia in Children Welfare Teaching Hospital. Type of the study: A cross-sectional study. Methods: This descriptive study was performed on 66 patients with thrombasthenia from the first of October 2013 till the first of July 2015.The diagnosis of the disease was done by a wide spectrum of characteristics including family history, clinical manifestations, laboratory tests.. Results: The common manifestations of the disease at time of diagnosis were epistaxis in 23 patients (34.8%) and gum bleeding in 22 patients (33.3%) .Mostly established at age 1-10years.Family history was positive in most patients.hepatitis C was rare in our patients after platelet transfutions. Conclusions: : It is a rare hemorrhagic disease in our center, mostly presented as minor bleeding involving mainly mucocutaneous regions which appears at an early childhood with positive family history in most cases.
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2016 |
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| Erschienen: |
2016 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:12 |
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| Enthalten in: |
مجله كليه طب الكندي - 12(2016), 2 |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
Lubna Foad Hussaia [VerfasserIn] |
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| Links: |
doaj.org [kostenfrei] |
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| Themen: |
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| Förderinstitution / Projekttitel: |
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| PPN (Katalog-ID): |
DOAJ078896452 |
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| 520 | |a Background: Thrombasthenia is an inherited genetic disorder affecting platelets, which is characterized by spontaneous muco-cutaneous bleeding and abnormally prolonged bleeding in response to injury or trauma. Objectives: The aim of this study was to assess the diagnosis and treatment of thrombasthenia in Children Welfare Teaching Hospital. Type of the study: A cross-sectional study. Methods: This descriptive study was performed on 66 patients with thrombasthenia from the first of October 2013 till the first of July 2015.The diagnosis of the disease was done by a wide spectrum of characteristics including family history, clinical manifestations, laboratory tests.. Results: The common manifestations of the disease at time of diagnosis were epistaxis in 23 patients (34.8%) and gum bleeding in 22 patients (33.3%) .Mostly established at age 1-10years.Family history was positive in most patients.hepatitis C was rare in our patients after platelet transfutions. Conclusions: : It is a rare hemorrhagic disease in our center, mostly presented as minor bleeding involving mainly mucocutaneous regions which appears at an early childhood with positive family history in most cases | ||
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