lamellar ichthyosis newsletter

Lamellar Ichthyosis (LI) is an autosomal recessive congenital Ichthyosis (ARCI), which mainly affects the skin. It is a clinically and genetically heterogeneous group of dermatological scaly skin disorders. Unfortunately, the condition has no cure.

DelveInsight, through its newsletter, brings to focus the rare genetic skin disorders present at the time of birth. Our newsletter lays down a brief introduction of the condition, its manifestations, etiology, and diagnosis. Lamellar ichthyosis is a rare and chronic genetic skin disorder that falls under the broader category of congenital ichthyoses, a group of disorders characterized by scaly skin due to abnormal keratinization. The term "lamellar" refers to the large, plate-like scales that are often brown or dark gray and cover much of the body surface. This condition is typically present at birth and persists throughout life, although severity may vary among individuals.

The newsletter also focuses on treatment modalities being followed for Lamellar Ichthyosis, unmet needs prevalent in the Lamellar Ichthyosis Market, and the affected population. It also compiles happenings on the news front, Lamellar Ichthyosis emerging therapies, and international organizations supporting the affected patients, its R&D with a gist of ongoing clinical trials.

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Want to explore more? Visit our infographics section for latest updates on Lamellar Ichthyosis treatment landscape