centrofacial lentiginosis

cen·tro·fa·cial len·tig·i·no·sis

[MIM*151000 & MIM*151001]
uncommon autosomal dominant syndrome of small hyperpigmented macules in a horizontal band across the center of the face at 1 year, increasing in number up to 10 years, and associated with skeletal and neural defects.
References in periodicals archive ?
There are few case reports of nevus spilus associated with other abnormalities like halo nevus,5 centrofacial lentiginosis,6 bilateral nevus of Ito7 etc.