[A rare case of incomplete Crist-Siemens syndrome].
D000013:Congenital Abnormalities; D004476:Ectodermal Dysplasia; D006801:Humans; D007642:Keratosis; D012873:Skin Diseases, Genetic; D014071:Tooth Abnormalities
ABNORMALITIES; ECTODERMAL DYSPLASIA; TEETH/abnormalities
Su di un raro caso di sindrome di Crist-Siemens spuria.