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

Journal of Pediatric Hematology/Oncology

Volumn 38, Issue 8, 2016, Pages 661-662

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

^a ULUDAG UNIVERSITY   (Turkey)

Author keywords

hemophagocytic lymphohistiocytosis; LCHAD deficiency; liver failure

Indexed keywords

CREATINE KINASE; MITOCHONDRIAL TRIFUNCTIONAL PROTEIN;

CASE REPORT; CLINICAL FEATURE; CREATINE KINASE BLOOD LEVEL; DIFFERENTIAL DIAGNOSIS; FEMALE; GENE MUTATION; HEMOPHAGOCYTIC SYNDROME; HUMAN; HYPOGLYCEMIA; INFANT; LABORATORY DIAGNOSIS; LIVER FAILURE; METABOLIC ACIDOSIS; MULTIPLE ACYL COA DEHYDROGENASE DEFICIENCY; MUTATIONAL ANALYSIS; PANCYTOPENIA; PRIORITY JOURNAL; REVIEW; RHABDOMYOLYSIS; ACIDOSIS; CARDIOMYOPATHIES; DEFICIENCY; DNA MUTATIONAL ANALYSIS; GENETICS; LIPID METABOLISM, INBORN ERRORS; LYMPHOHISTIOCYTOSIS, HEMOPHAGOCYTIC; MITOCHONDRIAL MYOPATHIES; NERVOUS SYSTEM DISEASES;

ACIDOSIS; CARDIOMYOPATHIES; CREATINE KINASE; DIAGNOSIS, DIFFERENTIAL; DNA MUTATIONAL ANALYSIS; HUMANS; HYPOGLYCEMIA; INFANT; LIPID METABOLISM, INBORN ERRORS; LYMPHOHISTIOCYTOSIS, HEMOPHAGOCYTIC; MITOCHONDRIAL MYOPATHIES; MITOCHONDRIAL TRIFUNCTIONAL PROTEIN; NERVOUS SYSTEM DISEASES; RHABDOMYOLYSIS;

EID: 84994672072     PISSN: 10774114     EISSN: 15363678     Source Type: Journal    
DOI: 10.1097/MPH.0000000000000626     Document Type: Review

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