X-linked reticulate pigmentary disorder
RARE X-LINKED GENETIC CONDITION
Partington amyloidosis; Partington cutaneous amyloidosis; Reticulate pigmentary disorder; Familial cutaneous amyloidosis; Partington syndrome type II; X-linked reticulate pigmentary disorder with systemic manifestations
X-linked reticulate pigmentary disorder is a rare X-linked genetic condition in which males manifest multiple systemic symptoms and a reticulated mottled brown pigmentation of the skin, which, on biopsy, demonstrated dermal deposits of amyloid. Females usually only have linear streaks of hyperpigmentation.