Publications by authors named "Tenagne Million"

Article Synopsis
  • Gastroschisis and omphalocele are common abdominal wall defects in newborns that can lead to serious health issues, and managing them effectively remains a challenge despite surgical advancements.!
  • The retrospective study at Tikur Anbessa Specialized Hospital examined 50 neonates with these defects between August 2018 and August 2022, noting a higher incidence of associated malformations in omphalocele cases compared to gastroschisis.!
  • Results indicated a higher mortality rate in gastroschisis cases (11 deaths) compared to omphalocele, with sepsis being the main cause of death, highlighting the need for improved management strategies in neonatal care.!
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Sickle cell disease (SCD) is a hereditary blood disorder characterized by abnormal hemoglobin, resulting in various clinical manifestations. Recognizing the complex clinical picture of SCD is crucial for physicians to effectively diagnose and manage the disease. While typical presentations may be absent, it is important to consider the possibility of SCD in patients presenting with ulcerative colitis (UC).

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