Hydrops fetalis and early neonatal multiple organ failure in familial hemophagocytic lymphohistiocytosis

European Journal of Medical Genetics

Volumn 52, Issue 6, 2009, Pages 417-420

  Vermeulen, Marijn J ^a   de Haas, Valerie ^a   Mulder, Margot F ^a   Flohil, Claudie ^a   Fetter, Willem P F ^a   van de Kamp, Jiddeke M ^a  

^a VU UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

Hemophagocytic lymphohistiocytosis; Hydrops fetalis; Multiple organ failure; Neonate; Perforin; PRF1

Indexed keywords

PERFORIN;

ARTICLE; AUTOPSY; CASE REPORT; DISEASE ASSOCIATION; DNA DETERMINATION; FEMALE; FETUS HYDROPS; GENE MUTATION; HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS; HISTOLOGY; HUMAN; MALE; MEDICAL LITERATURE; MULTIPLE ORGAN FAILURE; NEWBORN; SIBLING;

FATAL OUTCOME; FEMALE; HETEROZYGOTE; HUMANS; HYDROPS FETALIS; INFANT, NEWBORN; LYMPHOHISTIOCYTOSIS, HEMOPHAGOCYTIC; MALE; MULTIPLE ORGAN FAILURE; MUTATION;

EID: 70350619192     PISSN: 17697212     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejmg.2009.07.002     Document Type: Article

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