Handbook of Pediatric Retinal OCT and the Eye-Brain Connection
Incontinentia pigmenti
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, Chapter
Toth, CA
January 1, 2019
Incontinentia pigmenti (IKBKG/NEMO gene-related retinopathy, Bloch-Sulzberger syndrome) is an X-linked dominant disorder characterized by abnormalities of the skin, teeth, nails, hair, retina, and central nervous system (CNS) and usually lethal before birth in males. In this chapter, we discuss the clinical features, brain connection, OCT features, ancillary testing, and treatment for incontinentia pigmenti.
Duke Scholars
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Toth, C. A. (2019). Incontinentia pigmenti. In Handbook of Pediatric Retinal OCT and the Eye-Brain Connection (pp. 145–148). https://doi.org/10.1016/B978-0-323-60984-5.00030-5
Toth, C. A. “Incontinentia pigmenti.” In Handbook of Pediatric Retinal OCT and the Eye-Brain Connection, 145–48, 2019. https://doi.org/10.1016/B978-0-323-60984-5.00030-5.
Toth CA. Incontinentia pigmenti. In: Handbook of Pediatric Retinal OCT and the Eye-Brain Connection. 2019. p. 145–8.
Toth, C. A. “Incontinentia pigmenti.” Handbook of Pediatric Retinal OCT and the Eye-Brain Connection, 2019, pp. 145–48. Scopus, doi:10.1016/B978-0-323-60984-5.00030-5.
Toth CA. Incontinentia pigmenti. Handbook of Pediatric Retinal OCT and the Eye-Brain Connection. 2019. p. 145–148.