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Handbook of Pediatric Retinal OCT and the Eye-Brain Connection

Incontinentia pigmenti

Publication ,  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

DOI

ISBN

9780323609852

Publication Date

January 1, 2019

Start / End Page

145 / 148
 

Citation

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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.
Journal cover image

DOI

ISBN

9780323609852

Publication Date

January 1, 2019

Start / End Page

145 / 148