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
APA
Chicago
ICMJE
MLA
NLM
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.
DOI
ISBN
9780323609852
Publication Date
January 1, 2019
Start / End Page
145 / 148