Results 1 to 10 of about 4,853 (113)

Simple virilizing form of 21-hydroxylase deficiency presenting with renal Insufficiency and polycythemia: a case report [PDF]

open access: yesFrontiers in Endocrinology
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
doaj   +2 more sources

Polycythemia and its determinants among children with unoperated cyanotic congenital heart disease at Tikur Anbessa specialized hospital, Ethiopia: observational cross-sectional study [PDF]

open access: yesBMC Pediatrics
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]

open access: yesHaematologica
Not available.
Paulo Siqueira do Amaral   +2 more
doaj   +2 more sources

Double-Outlet Right Ventricular Malformation in a Two-Year-Old Aberdeen Angus Cow [PDF]

open access: yesAnimals
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
doaj   +2 more sources

Surviving Unrepaired Tetralogy of Fallot to 43 Years in a Low-Resource Setting: The Oldest Reported Case from Somalia [PDF]

open access: yesInternational Medical Case Reports Journal
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
doaj   +2 more sources

Polycythemia Secondary to Pheochromocytoma

open access: yesJournal of Rawalpindi Medical College, 2021
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

Diagnosis and genetic analysis of polycythemia in children and a novel EPAS1 gene mutationWhat is knownWhat is new?

open access: yesPediatrics and Neonatology, 2022
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

A Rare Case of Congenital Methemoglobinemia with secondary polycythemia- Case Report and Literature Review

open access: yesHaematology Journal of Bangladesh, 2020
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
doaj   +1 more source

A CASE OF POLYCYTHEMIA DIAGNOSED AS HEMOGLOBIN ANDREW-MINNEAPOLIS

open access: yesHematology, Transfusion and Cell Therapy, 2021
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

open access: yesJournal of Nobel Medical College, 2023
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
doaj   +1 more source

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