Incontinentia pigmenti in a child with suspected retinoblastoma

Abstract

BACKGROUND Incontinentia pigmenti is a rare X-linked dominant syndrome caused by mutation in the NEMO/IKKgamma gene, and characterized by a spectrum of cutaneous, ocular, neurologic and dental abnormalities. In the eye, findings include retinal vascular non-perfusion, occasionally with traction retinal detachment, retinal fibrosis, and retinal pigment… (More)
DOI: 10.1186/s40942-017-0088-5

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