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).

Nasolacrimal duct obstruction

Blockage of the lacrimal duct.

Total: 2

(per page)

PMID (PMCID)
6521980	FEMALE	Infant
	Incontinentia pigmenti associated with nasolacrimal duct obstruction.
	Smith B, Bedrossian EH Jr. Ophthalmic Surg. 1984;15(12):980-2.
	This case is believed to be the first reported instance of incontinentia pigmenti associated with nasolacrimal duct obstruction.
6521980	FEMALE	Infant
	Incontinentia pigmenti associated with nasolacrimal duct obstruction.
	Smith B, Bedrossian EH Jr. Ophthalmic Surg. 1984;15(12):980-2.
	A case is reported of a five-month-old female with incontinentia pigmenti associated with nasolacrimal duct obstruction.