Results 1 to 10 of about 89,418 (239)
A Novel Alpha1‐Variant (HBA1:c.‐35T>C) Complexed With the First Reported Hb M‐Saskatoon in the Chinese Population [PDF]
Molecular Genetics & Genomic MedicineBackground Hemoglobinopathies are genetic disorders characterized by structural or quantitative hemoglobin abnormalities. We report the first documented case globally of a novel alpha1 (α1)‐variant (HBA1:c.‐35T>C) co‐occurring with Hb M‐Saskatoon (HBB:c ...
Yujing Yang +5 more
doaj +2 more sources
Cyanosis in a patient with atrial septal defect
Journal of the Practice of Cardiovascular Sciences, 2015 Cyanosis in ASD has multiple causes requiring etiology directed management. Cyanosis can present in the setting of elevated pulmonary artery pressure, as in Eisenmenger syndromes having a poor prognosis.
Vikas Thakran, Anunay Gupta
doaj +2 more sources
Anesthesiology, 1961 Combined effects of the factors contributing to the presence of reduced hemoglobin in the capillary blood ................................................... A .
C. Lundsgaard, D. D. van Slyke
openaire +2 more sources
Case report of congenital methemoglobinemia: an uncommon cause of neonatal cyanosis
Maternal Health, Neonatology and Perinatology, 2022 Background Methemoglobinemia can be an acquired or congenital condition. The acquired form occurs from exposure to oxidative agents. Congenital methemoglobinemia is a rare and potentially life-threatening cause of cyanosis in newborns that can be caused ...
A. Lyle +6 more
semanticscholar +1 more source
European Journal of Cardio-Thoracic Surgery, 2021 OBJECTIVES The Fontan operation aims at reducing cyanosis and cardiac volume overload in patients with complex univentricular heart malformations. However, persisting or reoccurring cyanosis is frequently observed.
Marie Schafstedde +6 more
semanticscholar +1 more source
A rare cause of cyanosis: Congenital methemoglobinemia
Clinical Case Reports, 2021 Congenital Methemoglobinemia is a rare condition that may mimic congenital heart diseases. There are two types of congenital Methemoglobinemia. The type I is usually benign. The enzyme deficiency is limited to red blood cells.
R. Guedri +3 more
semanticscholar +1 more source
A rare cause of cyanosis in neonatal age: Cor triatriatum dexter
Annals of Pediatric Cardiology, 2022 Cor triatriatum dexter is an extremely rare congenital anomaly that is caused by the partitioning of the right atrium by a broad sheet of tissue due to the persistence of the right sinus venosus valve.
Adriano Caputo +4 more
doaj +1 more source
A Hemoglobin Variant Associated with Neonatal Cyanosis and Anemia
New England Journal of Medicine, 2011 Todd L Mollan +2 more
exaly +2 more sources
Surviving fatal Methemoglobinemia [PDF]
Asia Pacific Journal of Medical Toxicology, 2023 Background: Methemoglobinemia is one of the rare causes of cyanosis, encountered in the Emergency Department. It can be congenital or acquired, affecting the oxygen binding capacity of hemoglobin, thus shifting the oxyhemoglobin dissociation curve to the
Irtiqa Sheikh +4 more
doaj +1 more source
Neonatal Outcome of Choanal Atresia Surgical Corrections- Experience from a Tertiary Care Centre from Eastern India [PDF]
Journal of Clinical and Diagnostic Research, 2021 Choanal atresia is a congenital condition that occurs due to developmental failure of nasal cavity to communicate with the nasopharynx. There can be both unilateral and bilateral occlusion, bony, soft tissue and both. It can present at birth or early in
Bhabesh Kant Chowdhry +4 more
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