It’s one of the rarest — and most devastating — genetic disorders doctors encounter. Harlequin ichthyosis affects just a handful of newborns each year in the US, but the condition is unmistakable, ...

Tape-strip RNA sequencing identifies shared Th17/Th22 upregulation and epidermal differentiation complex activation across ...

Harlequin ichthyosis (HI) is a rare, severe genetic skin disorder caused by ABCA12 mutations, leading to defective lipid transport and loss of skin barrier function. Infants present with thick, ...

Please provide your email address to receive an email when new articles are posted on . The Ichthyosis Scoring System was developed to quantify ichthyosis severity across body sites. The system ...