ichthyosiform erythroderma造句

• Children who survive the neonatal period usually evolve to a less severe phenotype, resembling a severe congenital ichthyosiform erythroderma.
• "' Congenital hemidysplasia with ichthyosiform erythroderma and limb defects "'( also known as " CHILD syndrome " ) is a genetic disorder with onset at birth seen almost exclusively in females.
• Deletions of " Alox12b " or " Aloxe3 " genes by gene knockout in mice cause a congenital scaly skin disease which is characterized by a greatly reduced skin water barrier function and other features found in the autosomal recessive nonbullous Congenital ichthyosiform erythroderma ( ARCI ) disease of humans .; ARCI refers to nonsyndromic ( i . e . not associated with other signs or symptoms ) congenital Ichthyosis including Harlequin-type ichthyosis, Lamellar ichthyosis, and Congenital ichthyosiform erythroderma.
• Deletions of " Alox12b " or " Aloxe3 " genes by gene knockout in mice cause a congenital scaly skin disease which is characterized by a greatly reduced skin water barrier function and other features found in the autosomal recessive nonbullous Congenital ichthyosiform erythroderma ( ARCI ) disease of humans .; ARCI refers to nonsyndromic ( i . e . not associated with other signs or symptoms ) congenital Ichthyosis including Harlequin-type ichthyosis, Lamellar ichthyosis, and Congenital ichthyosiform erythroderma.