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

Author:

Alla Sai Santhosha Mrudula1,Agarwal Pahel2,Shah Dhruv J.3,Shajahan Waseem Abrar4,Ramsundar Rakshna5,Alla Deekshitha1ORCID,Ravulapalli Madhavi2,Bora Satya6,Pillai Sanjay7,Bayeh Ruth G.8ORCID,Repalle Uday Kumar6,Suhani Fnu9

Affiliation:

1. Andhra Medical College Visakhapatnam India

2. Bhaskar Medical College Hyderabad India

3. Massachusetts College of Pharmacy and Health Sciences Boston Massachusetts USA

4. Government Medical College Kozhikode Kozhikode India

5. Sri Ramachandra Institute of Higher Education and Research (Deemed to be University) Chennai India

6. Dr Pinnamaneni Siddhartha Institute of Medical Sciences and Research Foundation Chinna Avutapalle India

7. MS Ramaiah Medical College Bengaluru India

8. Adama General Hospital and Medical College Nazret Ethiopia

9. Dayanand Medical College and Hospital Ludhiana India

Abstract

Key Clinical MessageHeme 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.

Publisher

Wiley

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