severe anemia due to parvovirus b19 in a silver haired boy
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ID: 225714
2016
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Abstract
Griscelli syndrome (GS) is a rare autosomal recessive immunodeficiency disorder in which the affected children present with characteristic silvery-white hairs. The hair microscopy of these children is characteristic and is helpful in differentiating GS from Chediak-Higashi syndrome which also presents with immunodeficiency and silver hairs. We report a 17-month-old boy with GS type 2 who presented with severe anemia. Bone marrow examination of the child suggested parvovirus B19 as the cause of severe anemia, which was later confirmed by DNA polymerase chain reaction.
| Reference Key |
verma2016indiansevere
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|---|---|
| Authors | ;Nishant Verma;Archana Kumar;Rashmi Kushwaha |
| Journal | journal of materials processing technology |
| Year | 2016 |
| DOI |
10.4103/0377-4929.178228
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