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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ژورنال

عنوان ژورنال: International Journal of Contemporary Pediatrics

سال: 2021

ISSN: ['2349-3283', '2349-3291']

DOI: https://doi.org/10.18203/2349-3291.ijcp20212063