KLICK syndrome: an overlooked form of congenital ichthyosis.
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DOI:
https://doi.org/10.26326/2281-9649.34.3.2653How to Cite
Mouhsine Z., Hali F., Allali R., Marnissi F., Chiheb S. 2024. KLICK syndrome: an overlooked form of congenital ichthyosis. Eur. J. Pediat. Dermatol. 34 (3):164-6. 10.26326/2281-9649.34.3.2653.
pp. 164-6
Abstract
KLICK syndrome is a rare autosomal recessive inherited skin disorder linked to abnormal epidermal keratinization. It is characterized by transgrediens palmar plantar keratoderma, congenital ichthyosis and linear hyperkeratotic plaques. The case of a 21-year-old patient who presented with desquamation all over the skin and hyperkeratosis of the large folds since birth was reported.
Keywords
ichthyosis, CLICK syndrome