Harlequin ichthyosis (HI) is the most severe type of congenital ichthyosis, and it is extremely rare. It is inherited in an autosomal recessive fashion. Although previously thought to be lethal, recently there have been increased reports of prolonged survival, following improved supportive care and judicious use of systemic retinoids. We report a new case of HI in an infant born of a consanguineous marraige who succumbed on the 5th day of birth despite intensive supportive care, a short review of literature regarding the condition is also presented
Abstract Harlequin ichthyosis is a rare autosomal recessive congenital ichthyosis with a distinct ph...
Harlequin ichthyosis is a severe and usually fatal congenital keratinization disorder. Although it h...
Abstract Harlequin ichthyosis is a rare autosomal recessive disorder occurring in 1: 3,000,000 birth...
Harlequin Ichthyosis is the most serious congenital keratinization disorder. When the children are b...
Harlequin fetus is a rare and the most severe genetic form of the congenital ichthyosis with an auto...
ABSTRACT Harlequin Ichthyosis is the most severe form of congenital ichthyosis. It characteristica...
Harlequin ichthyosis is a rare congenital ichthyosis classified under the category of Autosomal Rece...
Harlequin ichthyosis is the most severe form of autosomal-recessive congenital ichthyoses with a hig...
Harlequin ichthyosis (HI) is a genetically inherited epidermal disorder due to the mutation of the A...
Harlequin ichthyosis is a rare, severe formof ichthyosis, which presents at birth. The neonate is en...
Harlequin Ichthyosis is the most severe form of congenital Ichthyosis presenting at birth. It is a v...
Harlequin ichthyosis (HI), a rare severe form of congenital ichthyosis is caused by recessive mutati...
Harlequin ichthyosis (HI) is a rare and severe form of congenital ichthyosis caused by truncating mu...
Harlequin ichthyosis is a very rare condition that affects the skin of newborns. It is associated wi...
Harlequin ichthyosis is a rare and severe genetic skin disorder that occurs within the developing fo...
Abstract Harlequin ichthyosis is a rare autosomal recessive congenital ichthyosis with a distinct ph...
Harlequin ichthyosis is a severe and usually fatal congenital keratinization disorder. Although it h...
Abstract Harlequin ichthyosis is a rare autosomal recessive disorder occurring in 1: 3,000,000 birth...
Harlequin Ichthyosis is the most serious congenital keratinization disorder. When the children are b...
Harlequin fetus is a rare and the most severe genetic form of the congenital ichthyosis with an auto...
ABSTRACT Harlequin Ichthyosis is the most severe form of congenital ichthyosis. It characteristica...
Harlequin ichthyosis is a rare congenital ichthyosis classified under the category of Autosomal Rece...
Harlequin ichthyosis is the most severe form of autosomal-recessive congenital ichthyoses with a hig...
Harlequin ichthyosis (HI) is a genetically inherited epidermal disorder due to the mutation of the A...
Harlequin ichthyosis is a rare, severe formof ichthyosis, which presents at birth. The neonate is en...
Harlequin Ichthyosis is the most severe form of congenital Ichthyosis presenting at birth. It is a v...
Harlequin ichthyosis (HI), a rare severe form of congenital ichthyosis is caused by recessive mutati...
Harlequin ichthyosis (HI) is a rare and severe form of congenital ichthyosis caused by truncating mu...
Harlequin ichthyosis is a very rare condition that affects the skin of newborns. It is associated wi...
Harlequin ichthyosis is a rare and severe genetic skin disorder that occurs within the developing fo...
Abstract Harlequin ichthyosis is a rare autosomal recessive congenital ichthyosis with a distinct ph...
Harlequin ichthyosis is a severe and usually fatal congenital keratinization disorder. Although it h...
Abstract Harlequin ichthyosis is a rare autosomal recessive disorder occurring in 1: 3,000,000 birth...