Publications by authors named "Huda Daood"

Article Synopsis
  • Acute hemorrhagic leukoencephalopathy (AHLE) is a rare and severe neurological condition with unclear causes, high morbidity, and significant mortality rates, but a case of a surviving young girl demonstrates potential for recovery.
  • A 13-year-old girl, after being treated for an upper respiratory infection, exhibited symptoms like drowsiness and received various treatments, including antiviral medications and IV immunoglobulin, which ultimately led to a diagnosis of AHLE.
  • The report emphasizes the challenge of accurately diagnosing AHLE due to its similarity to other more common neurological diseases, highlighting the need for more research into this rare condition.
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Article Synopsis
  • Early detection and treatment of total anomalous pulmonary venous connection (TAPVC) are crucial for improving outcomes, as showcased by a 7-month-old patient diagnosed after experiencing cyanotic episodes.
  • TAPVC is a rare congenital heart defect characterized by abnormal blood flow, with the infracardiac subtype presenting a risk of obstruction and often diagnosed in newborns.
  • Successful surgical intervention and a stable recovery in this case highlight the need for thorough newborn exams and timely referrals to specialists to address this serious condition effectively.
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Kartagener syndrome is a rare, autosomal recessive genetic disorder that causes defects in the action of ciliary movement, comprises of triad situs inversus, chronic sinusitis, and bronchiectasis. We present the case of a 3-year-old boy with repeated respiratory infections and pneumonic infections presenting with acute respiratory failure. He was diagnosed with Kartagener syndrome based on his clinical presentation and imaging features.

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