Symptoms include: Keratosis pilaris atrophicans faciei (KPAF) is a rare, hereditary subtype of keratosis pilaris. The onset of symptoms most commonly occurs in infancy and early childhood.

Keratosis pilaris atrophicans faciei (ulerythema ophryogenes) has been described as a cutaneous marker for several congenital syndromes. To our knowledge, its possible association with Cornelia de ...