{Reference Type}: Letter
{Title}: Spontaneous clinical remission of Nagashima-type palmoplantar keratoderma in a patient of Korean descent with a heterozygous SERPINB7 mutation.
{Author}: Thakker S;Owusu-Agyei M;Marchalik R;Kang JK;
{Journal}: Pediatr Dermatol
{Volume}: 41
{Issue}: 2
{Year}: 2024 Mar-Apr 2
{Factor}: 1.997
{DOI}: 10.1111/pde.15511
{Abstract}: Nagashima-type palmoplantar keratoderma (NPPK) is an autosomal recessive form of diffuse palmoplantar keratoderma (PPK) characterized by thickening and redness of palms and/or soles. In this report, we describe a female patient of Korean descent who had clinical remission of her adult-onset NPPK. To our knowledge, she is the first reported heterozygous SERBINB7 mutation carrier to present with classic NPPK who achieved spontaneous clinical remission.