Simple virilizing form of 21-hydroxylase deficiency presenting with renal Insufficiency and polycythemia: a case report [PDF]
The simple virilizing (SV) form of 21-hydroxylase deficiency (21-OHD) is primarily characterized by androgen excess. Gonadal dysfunction is widely acknowledged; however, systemic complications, including renal injury, are often overlooked.
Lu Liang +6 more
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Polycythemia and its determinants among children with unoperated cyanotic congenital heart disease at Tikur Anbessa specialized hospital, Ethiopia: observational cross-sectional study [PDF]
Background Polycythemia is a physiologic adaptive response to hypoxia seen in children with cyanotic congenital heart disease (Cyanotic CHD). Globally, due to timely cyanotic CHD interventions, polycythemia is underreported or understudied.
Lelise Kaba, Henok Tadele
doaj +2 more sources
von Hippel-Lindau syndrome-related congenital polycythemia and response to belzutifan [PDF]
Not available.
Paulo Siqueira do Amaral +2 more
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Double-Outlet Right Ventricular Malformation in a Two-Year-Old Aberdeen Angus Cow [PDF]
A 2-year-old Aberdeen Angus cow was presented with lethargy and decreased appetite at the VA-MD College of Veterinary Medicine Large Animal Teaching Hospital.
Baker White +5 more
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Surviving Unrepaired Tetralogy of Fallot to 43 Years in a Low-Resource Setting: The Oldest Reported Case from Somalia [PDF]
Abdirahman A Warfaa,1 Abdirahman Ibrahim Said,1 Mohamoud Abdulahi,1 Mohamed Said Hassan1,2 1College of Health Science, School of Medicine, Amoud University, Borama, Somalia; 2School of Postgraduate Studies and Research, Amoud University, Borama ...
Warfaa AA +3 more
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Polycythemia Secondary to Pheochromocytoma
Polycythemia, also known as polyglobulia, is a clinical condition characterized by an increased number of red blood cells (RBC) or haematocrit concentrations in the peripheral blood. It can either be primary (polycythemia vera) or secondary, which can be
Raheel Raza +4 more
doaj +1 more source
Background: Unlike in adults, there is no consensus on management and diagnosis of polycythemia in children. This study aims to evaluate the diagnosis and verify the algorithm in children with polycythemia.
Hatice Mine Cakmak +3 more
doaj +1 more source
Congenital heart diseases are common cause of congenital cyanosis with polycythaemia. Congenital methemoglobinemia is a rare cause of lifelong cyanosis with polycythemia.
Tasneem Ara +2 more
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A CASE OF POLYCYTHEMIA DIAGNOSED AS HEMOGLOBIN ANDREW-MINNEAPOLIS
Objective: Polycythemia is a rare condition in which an increase in erythrocyte mass is observed. It can be primary or secondary. Primary polycythemia occurs as a result of congenital or acquired mutations that regulate erythroid development.
Mustafa Bilici +9 more
doaj +1 more source
Immediate Outcomes in Neonates Born to Diabetic Mothers
Background: Infants born to diabetic mothers are at a higher risk of developing complications like macrosomia, hypoglycemia, hypocalcemia, hypomagnesemia, polycythemia, hyperbilirubinemia, prematurity, transient tachypnea of newborn, respiratory distress
Vijay Kumar Sah +3 more
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