Incontinentia pigmenti

Incontinentia pigmenti (IP) is a rare X-linked dominant multi-systemic ectodermal dysplasia usually lethal in males and presenting neonatally in females with a bullous rash along Blashko's lines (BL) followed by verrucous plaques evolving over time to hyperpigmented swirling patterns. It is further characterized by teeth abnormalities, alopecia, nail dystrophy and affects occasionally the retina and the central nervous system (CNS).

Vitreous hemorrhage

Bleeding within the vitreous compartment of the eye.


Total: 1

                      


(per page)
PMID (PMCID)
28643725
(5508471)
FEMALE Child
A 7-year-old female child of incontinentia pigmenti presenting with vitreous hemorrhage.
Huang SY, Chen LJ, Chiu SC.
Indian J Ophthalmol. 2017;65(6):533-535.
A 7-year-old female child of incontinentia pigmenti presenting with vitreous hemorrhage.