Ontology highlight
ABSTRACT: Background
Congenital methemoglobinemia (metHb), a rare cause of neonatal cyanosis, results from the oxidation of ferrous to ferric iron in hemoglobin (Hb). The aim of this case report is to highlight the need to broaden the differential diagnosis of neonatal cyanosis and emphasizes the role of capillary blood gas analysis and genetic testing to exclude hereditary hematological causes. We report a previously unreported genetic mutation associated with congenital metHb.Case description
We report the case of a term male neonate with cyanosis unresponsive to oxygen administration. Complementary studies were normal, including echocardiography, cerebral ultrasound, blood tests, blood culture, cytomegalovirus testing, glucose-6-phosphate dehydrogenase (G6PD) assessment, and Hb el
SUBMITTER: Carmona-Nunez A
PROVIDER: S-EPMC11983008 | biostudies-literature | 2025 Mar
REPOSITORIES: biostudies-literature