An Unusual Case of LCHAD Deficiency Presenting With a Clinical Picture of Hemophagocytic Lymphohistiocytosis: Secondary HLH or Coincidence?

Author:

Erdol Sahin,Ture Mehmet,Baytan Birol,Yakut Tahsin,Saglam Halil

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Oncology,Hematology,Pediatrics, Perinatology, and Child Health

Reference7 articles.

1. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: clinical presentation and follow-up of 50 patients;Den Boer;Pediatrics,2002

2. Review of haemophagocytic lymphohistiocytosis;Freeman;Arch Dis Child,2011

3. Congenital galactosemia: an unusual presentation;Marcoux;Arch Pediatr,2005

4. Phenotypic continuum of type 2 Gaucher disease: an intermediate phenotype between perinatal-lethal and classic type 2 Gaucher disease;Ben Turkia;J Perinatol,2009

5. Two new cases with Pearson syndrome and review of Hacettepe experience;Topaloglu;Turk J Pediatr,2008

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1. Genetics of Acquired Cytokine Storm Syndromes;Advances in Experimental Medicine and Biology;2024

2. Secondary hemophagocytic lymphohistiocytosis in children (Review);Experimental and Therapeutic Medicine;2023-07-17

3. Rare diseases presenting with hemophagocytic lymphohistiocytosis;Pediatrics International;2023-01

4. Hemophagocytic Lymphohistiocytosis;Balkan Medical Journal;2022-09-09

5. Case Report: Hemophagocytic Lymphocytosis in a Patient With Glutaric Aciduria Type IIC;Frontiers in Immunology;2022-01-13

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