A rare case of heme oxygenase deficiency: A case report and literature review

Key Clinical Message Heme oxygenase deficiency, a rare condition disrupting heme metabolism, has only nine reported cases. We present a 3‐year‐old boy with dysmorphic facies, asplenia, and normal bilirubin levels despite ongoing hemolysis. Blood transfusions sustained hemoglobin while IV steroids ma...

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Veröffentlicht in:	Clinical Case Reports 2024-06, Vol.12 (6), p.e8986-n/a
Hauptverfasser:	Alla, Sai Santhosha Mrudula, Agarwal, Pahel, Shah, Dhruv J., Shajahan, Waseem Abrar, Ramsundar, Rakshna, Alla, Deekshitha, Ravulapalli, Madhavi, Bora, Satya, Pillai, Sanjay, Bayeh, Ruth G., Repalle, Uday Kumar, Suhani, Fnu
Format:	Artikel
Sprache:	eng
Schlagworte:	Abdomen Antibiotics Antihypertensives asplenia Bilirubin bilirubin synthesis Biopsy Blood coagulation factors Blood platelets Blood pressure Blood transfusion Blood transfusions Case reports Endothelium Enzymes Fever Genes Hematuria Heme heme oxygenase deficiency Hemoglobin HMOX1 gene Hypertension Literature reviews Metabolism Oxidative stress Physiological aspects Proteins
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Zusammenfassung:	Key Clinical Message Heme oxygenase deficiency, a rare condition disrupting heme metabolism, has only nine reported cases. We present a 3‐year‐old boy with dysmorphic facies, asplenia, and normal bilirubin levels despite ongoing hemolysis. Blood transfusions sustained hemoglobin while IV steroids managed inflammation.
ISSN:	2050-0904 2050-0904
DOI:	10.1002/ccr3.8986