Case report: A case of incontinentia pigmenti
Incontinentia pigmenti (IP) is a rare neuroectodermal dysplasia caused by mutations in the IKBKG gene. We present a case of a 4-month-old female infant with erythematous vesicular skin lesions on the trunk and extremities. Histopathologic examination of the blisters revealed an eosinophilic infiltra...
Main Authors: | , , , , , , , , |
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פורמט: | Article |
שפה: | English |
יצא לאור: |
Frontiers Media S.A.
2023-05-01
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סדרה: | Frontiers in Medicine |
נושאים: | |
גישה מקוונת: | https://www.frontiersin.org/articles/10.3389/fmed.2023.1164394/full |