Importance Olmsted syndrome is a genodermatosis characterized by painful and mutilating
palmoplantar keratoderma (PPK) that progresses from infancy onward and lacks an effective …

Importance Olmsted syndrome is a rare and disabling genodermatosis for which no
successful treatment is currently available. Objective To evaluate the clinical response to the …

Importance Olmsted syndrome (OS) is a rare keratinizing disorder characterized by
excessive epidermal thickening of the palms and soles, with clinical and genetic …

The patient has remained on erlotinib for 2 years in addition to oral retinoids and surgical
parings. Although she has not maintained her initial dramatic response, she continues to …

Olmsted syndrome (OS) is a rare congenital disorder characterized by palmoplantar and
periorificial keratoderma, alopecia in most cases, and severe itching. The genetic basis for …

Background Olmsted syndrome is a rare congenital skin disorder presenting with periorifical
hyperkeratotic lesions and mutilating palmoplantar keratoderma, which is often associated …

Olmsted syndrome (OS) is a rare keratinization disorder, typically characterized by two
primary diagnostic hallmarks—mutilating palmoplanter and periorificial keratoderma …

Olmsted syndrome (OS) is a rare congenital skin disorder characterized by severe
palmoplantar and periorificial keratoderma, alopecia, onychodystrophy, and severe pruritus …

DEAR EDITOR, Olmsted syndrome (OS; MIM# 614594), is a rare genetic skin disorder, with~
50 cases reported in the literature. 1 Most cases are sporadic although familial cases with …

Olmsted syndrome (OS) is a rare congenital skin disorder characterized by palmoplantar
keratoderma, periorificial hyperkeratotic lesions and alopecia. Constriction of digits …