Harlequin Ichthyosis - Get information and read articles on Harlequin Ichthyosis signs, symptoms, causes, treatment, prevention and diagnosis at onlymyhealth.com, your complete health guide.
Those born with harlequin ichthyosis have severe cranial and facial deformities. Hard, thick skin that covers the most of the body is the characteristic of the inherited skin condition.
Harlequin ichthyosis is a skin condition, the most severe form of congenital ichthyosis. The condition is characterized by a thickening of the keratin layer in foetal human skin.
Harlequin ichthyosis is an inherited disorder that mainly affects the skin. The rare skin disorder is inherited in an autosomal recessive pattern.
Harlequin Ichthyosis is a severe genetic disorder that mainly affects skin’s regeneration process. It is a rare skin disorder and one of the most severe ones
A loss of functional gene ABCA12 protein disrupts the normal development of the epidermis, resulting in the hard, thick scales characteristic of harlequin ichthyosis.