[On a case of unusual multiple congenital malformations].
D000013:Congenital Abnormalities / Q000209:etiology*; D006801:Humans; D012256:Riboflavin; D012257:Riboflavin Deficiency; D013577:Syndrome; D014802:Vitamin A Deficiency; D014804:Vitamin B Deficiency
D012256:Riboflavin
ABNORMALITIES/etiology and pathogenesis; VITAMIN A DEFICIENCY; VITAMIN B2 DEFICIENCY
Su di un caso di non comuni malformazioni multiple congenite.