Fetal keratoderma

Ittiosi congenita autosomico-recessiva (1) Autosomal recessive congenital ichthyosis (1) Premature infant (1) Infant, Premature (1) ATP binding cassette subfamily A member 12 gene mutation (1) Neonato pretermine (1) Harlequin ichthyosis (1) ABCA12 gene mutation (1) lipide transporter deficiency (1) congenital diffuse hyperkeratosis (1) Keratins (1) Cheratosi fetale (1) preterm birth (1) Ittiosi Arlecchino (1) ATP-Binding Cassette Transporters (1) premature birth (1) Ichthyosis, Lamellar (1) Arlecchino syndrome (1) Mutation (1) Gene ABCA12 (1)