Abstract
Incontinentia pigmenti (IP) is a rare multisystem genetic disorder affecting predominantly females. It is characterized by distinct cutaneous lesions with additional common abnormalities involving teeth, eyes and central nervous system. Here we present a case of IP with classical cutaneous lesions occurring in four stages with ocular involvement.
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Gondokaryono, S.P., Diana, I.A., Effendi, R.M.R.A., Dwiyana, R.F. (2022). Incontinentia Pigmenti with Ocular Involvement. In: Arcangeli, F., Lotti, T.M. (eds) Clinical Cases in Neonatal and Infant Dermatology. Clinical Cases in Dermatology. Springer, Cham. https://doi.org/10.1007/978-3-030-91523-0_24
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DOI: https://doi.org/10.1007/978-3-030-91523-0_24
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