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- W2211884906 abstract "Incontinentia pigmenti (IP; Bloch-Sulzberger syndrome) is an X-linked dominant genodermatosis that can have several cutaneous, dental, skeletal, neurologic, and ocular manifestations, including retinal detachment, seizures, paralysis, developmental delay, hair loss, and abnormal dentition.1-3 Lethal for affected males in utero, IP presents overwhelmingly in females as a result of mutant X chromosome inactivation.2 Lyonization of the X chromosome is what contributes to the reticular or whorled vesiculobullous pattern pathognomonic for IP." @default.
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- W2211884906 date "2015-11-01" @default.
- W2211884906 modified "2023-10-14" @default.
- W2211884906 title "A case of incontinentia pigmenti reactivation after 12-month immunizations" @default.
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- W2211884906 doi "https://doi.org/10.1016/j.jdcr.2015.08.009" @default.
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