21q22.11q22.12 deletion syndrome with secondary hemophagocytic lymphohistiocytosis
نویسندگان
چکیده
Haemophagocyticy lymyphohistiocytosis in the new-born is uncommon. Incidence reported between 1 50,000 to 1,50,000 admissions. Usually it primary or familial HLH first year of life. Secondary causes are due viral, bacterial and fungal infections. A dysmorphic small for gestational age male neonate presented with sepsis neonatal cholestasis. He also had associated HLH. Exom sequencing showed a 21q22.11q22.12 deletion. This has not known have any association was managed IVIG steroids. The made recovery but succumbed later an intercurrent illness.
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To the Editor: We found interesting the article by Lupo et al. about a case of fatal measles in an immunocompetent 29-yearold woman (Fatal measles without rash in immunocompetent adult, France; http://dx.doi.org/10.3201/ eid1803.111300). Perhaps, however, the possible diagnosis of secondary hemophagocytic lymphohistiocytosis (HLH) should also have been considered in that setting. HLH is a poten...
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ژورنال
عنوان ژورنال: International Journal of Contemporary Pediatrics
سال: 2021
ISSN: ['2349-3283', '2349-3291']
DOI: https://doi.org/10.18203/2349-3291.ijcp20212063