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).

Spinal deformities



Total: 1

                      


(per page)
PMID (PMCID)
23808269
FEMALE Young Adult
[Staged correction of spinal deformity in a patient with incontinentia pigmenti syndrome].
Baklanov AN, Kolesov SV, Shavyrin IA.
Vestn Ross Akad Med Nauk. 2013;(3):45-50.
[Staged correction of spinal deformity in a patient with incontinentia pigmenti syndrome].