Fig. 1From: Clinical and genetic characterization of a Chanarin Dorfman Syndrome patient born to diseased parentsPedigree of CDS family (a). Microphotographs of May-Grünwald-Giemsa buffy coats of patient III-1 showing Jordan’s anomaly (arrows); original magnification 1000× (b). Sequence analysis showing the c594insC (N209X) ABHD5 mutation identified in homozygous status in all family members affected by CDS (c)Back to article page