Please use this identifier to cite or link to this item: http://20.193.157.4:9595/xmlui/handle/123456789/4800
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dc.contributor.authorKulkarni, Shruti-
dc.contributor.authorAdya, Keshavmurthy A-
dc.contributor.authorJanagond, Ajit B-
dc.contributor.authorInamadar, Arun-
dc.date.accessioned2023-04-19T11:02:03Z-
dc.date.available2023-04-19T11:02:03Z-
dc.date.issued2022-
dc.identifier.urihttp://hdl.handle.net/123456789/4800-
dc.description.abstractNeonatal lupus erythematosus (NLE) occurs due to transplacental transfer of autoantibodies in newborns of mothers with clinical or subclinical collagen vascular diseases. Anti-Ro/SSA antibodies are strongly associated with NLE. Anti-La/SSB and anti-U1 -RNP antibodies are less frequent. Cutaneous and cardiac manifestations are prominent of NLE. Nearly half of the cases show either cutaneous or cardiac features, and 10% show both. Skin lesions may be congenital or develop within 12–16 weeks postpartumen_US
dc.language.isoenen_US
dc.publisherBLDE(DU)en_US
dc.subjectpolycyclicen_US
dc.subjectneonatal lupusen_US
dc.titleCoexistence of annular polycyclic, morpheaform and atrophic lesions in neonatal lupus erythematosusen_US
dc.typeArticleen_US
Appears in Collections:BMJ Case Reports

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