{Reference Type}: Case Reports
{Title}: Acropigmentation of Kitamura with immigration delay disease: A rare entity.
{Author}: Kumar S;Mahajan BB;Kamra N;Bhoyar PA;
{Journal}: Indian Dermatol Online J
{Volume}: 6
{Issue}: 3
{Year}: May-Jun 2015
暂无{DOI}: 10.4103/2229-5178.156415
{Abstract}: Reticulate acropigmentation of Kitamura (RAK) is a rare, autosomal dominant disorder first described in Japan characterised by a reticulate pattern of slightly atrophic, angulated, hyperpigmented macules affecting the acral areas of the body. We hereby report a case of RAK in a young Indian male with adermatoglyphia that has not been previously reported in the literature.