Ichthyosis prematurity syndrome

MONDO:0012089

Ichthyosis prematurity syndrome is a rare, syndromic congenital ichthyosis characterized by premature birth (at gestational weeks 30-32, in general) in addition to thick, caseous and desquamating epidermis, neonatal respiratory asphyxia, and persistent eosinophilia. After the perinatal period, a spontaneous improvement in the health of affected patients is observed and skin features (vernix caseosa-like scale) evolve into a mild presentation of flat follicular hyperkeratosis with atopy.

Also known as: IPS, congenital ichthyosis type 4, ichthyosis prematurity syndrome, idiopathic pneumonia syndrome, ichthyosis congenita 4, ichthyosis congenita IV, ichthyosis-prematurity syndrome

36 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by