Results 1 to 10 of about 73,689 (289)

A Novel Alpha1‐Variant (HBA1:c.‐35T>C) Complexed With the First Reported Hb M‐Saskatoon in the Chinese Population [PDF]

open access: yesMolecular Genetics & Genomic Medicine
Background 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   +3 more sources

Case Report: An Anomalous Left Hepatic Venous Connection in a Patient With Unexpected Cyanosis [PDF]

open access: goldFrontiers in Pediatrics, 2021
An anomalous left hepatic venous (LHV) connection is an extremely rare cardiac malformation, and left hepatic venous route abnormalities not associated with other cardiac lesions do not require surgical treatment because they are physiologically benign ...
Fanyan Luo, Haisong Bu
doaj   +2 more sources

A Cyanotic Dilemma: Nitrobenzene Poisoning—A Case Report [PDF]

open access: yesClinical Case Reports
Acquired methemoglobinemia can rarely be caused by acute nitrobenzene poisoning, presenting as oxygen‐unresponsive, life‐threatening hypoxia. We discuss a case of a 19‐year‐old female who attempted suicide through intentional nitrobenzene poisoning.
Janmejay Kumar Singh   +9 more
doaj   +2 more sources

Case Report: Clinical presentations of cyanosis associated with acquired methemoglobinemia in infants—a clinical challenge [PDF]

open access: yesFrontiers in Pediatrics
BackgroundCyanosis is a common clinical finding in infants and children. Particularly, central cyanosis can be associated with significant and potentially life-threatening diseases.
Lin Wang   +8 more
doaj   +2 more sources

Case Report: Hemoglobin titusville: a specific case of cyanosis [PDF]

open access: yesFrontiers in Cardiovascular Medicine
Hemoglobin Titusville is a rare low-oxygen-affinity hemoglobinopathy characterized by normal arterial partial pressure of oxygen but low oxygen saturation. In this study, we describe a case of hemoglobinopathy presenting as cyanosis. A 12-year-old female
Meng Zhang   +6 more
doaj   +2 more sources

Neonatal Outcome of Choanal Atresia Surgical Corrections- Experience from a Tertiary Care Centre from Eastern India [PDF]

open access: yesJournal 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
doaj   +1 more source

A rare cause of cyanosis in neonatal age: Cor triatriatum dexter

open access: yesAnnals 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

Surviving fatal Methemoglobinemia [PDF]

open access: yesAsia 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

Delayed presentation of partial anomalous systemic venous connection

open access: yesAnnals of Pediatric Cardiology, 2021
Anomalies of systemic venous connections are extremely rare. We describe the case of an asymptomatic 29-year-old woman who was found to have systemic desaturation in the peripartum period and referred to us for suspected cyanotic heart disease.
Bharath A Paraswanath   +4 more
doaj   +1 more source

Imaging Insights into Eisenmenger Syndrome: From Basics to Sophistication

open access: yesJournal of the Indian Academy of Echocardiography & Cardiovascular Imaging, 2021
We describe an unusual case of a large aortopulmonary window which was not very symptomatic and presented as Eisenmenger syndrome at the age of 20 years in a male patient.
Srilakshmi M Adhyapak   +4 more
doaj   +1 more source

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