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The Olmsted syndrome

International Journal of Dermatology, 1997
A 35‐year‐old man had a hyperkeratotic disorder of the palmoplantar skin since the age of 6 months. The palmoplantar keratoderma progressed to thick and warty hyperkeratotic plaques, which enlarged and formed verrucous lesions and deep fissures. The acral keratoderma gradually involved the dorsal surface of the hands and feet with flexion contractures ...
O L, Santos   +7 more
openaire   +2 more sources

Olmsted Syndrome

Advances in Neonatal Care, 2021
Background: Olmsted syndrome is a rare and complex skin disorder affecting 46 (published) infants as of 2012. The infants affected in this case were born premature at 28 weeks' gestation. Infants affected by this syndrome demonstrate numerous plaques on several specific areas of the skin.
Sara, Anderson   +2 more
openaire   +2 more sources

Olmsted syndrome with microtia

European Journal of Pediatric Dermatology, 2021
Olmsted syndrome is a rare inherited skin disorder characterized by severe palmoplantar keratoderma associated with periorificial keratoderma. The actual report describes a case of this syndrome in a 3-year-old girl, who presents, in addition to the classic manifestations, microtia and preauricular appendage as a possible association.
Chandramohan, A., Kar, H.K.
openaire   +1 more source

Olmsted Syndrome

JAMA Dermatology
This case report describes a 6-year-old girl who presented with symmetrical massive keratotic plaques on the palms, soles, and perioral area, as well as hair loss for 4 years.
Yu-Ying, Huang, Jiu-Hong, Li
openaire   +2 more sources

Olmsted syndrome—a rare syndrome with oral manifestations

Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology, 2004
Olmsted syndrome is a rare, congenital condition characterized by severe palmo-planter keratosis, periorificial keratosis, and hypotrichosis. Though orofacial keratosis is one of the consistent findings of Olmsted syndrome, it has never been reported in the dental literature.
Puneet, Batra, Naseem, Shah
openaire   +3 more sources

Partial Improvement of Olmsted Syndrome With Etretinate

Pediatric Dermatology, 1993
Abstract: An 11‐year‐old Japanese boy with Olmsted syndrome was seen at our clinic. He had a sharply marglnated, painful keratoderma with a red border on his palms and soles. Flexion contractures of the fingers were also observed. Hyperkeratotic plaques were present below the lower lip, on the elbows and knees, and In the sacral area.
M, Ueda   +4 more
openaire   +2 more sources

Olmsted Syndrome in Twins

Archives of Dermatology, 1995
Olmsted syndrome is a rare disorder of keratinization appearing at birth or in early infancy that is characterized by the unusual association of palmoplantar keratoderma and periorificial hyperkeratosis, with possible involvement of other ectodermal derivatives.1-6We report the second familial case, showing a progressive course unresponsive to ...
openaire   +1 more source

Olmsted syndrome—congenital palmoplantar and periorificial keratoderma

Journal of the American Academy of Dermatology, 1984
We are reporting the third case of the Olmsted syndrome, an entity that has received little attention in the medical literature. The syndrome consists of congenital diffuse, sharply marginated keratoderma of the palms and soles, onychodystrophy , constrictions of digits, and periorificial keratoses.
Y, Poulin, H O, Perry, S A, Muller
openaire   +2 more sources

Olmsted syndrome: report of a new case

British Journal of Dermatology, 1997
We report the case of a 20-year-old man, who was born with an intense erythema of the genital area, unresponsive to any treatment employed. When he was 9 months old, he presented with well-defined hyperkeratotic erythematous plaques around the mouth, eyes, nose, and perianal area, with similar plaques on the lateral aspect of the neck and axillae.
J, Frias-Iniesta   +3 more
openaire   +2 more sources

Anesthetic management of a child with olmsted's syndrome

Journal of Anesthesia, 1994
In 1927, Olmsted described a 5-year-old boy in whom palmoplantar keratoderma had developed during the second half of his first year of life, and who later presented with circumnasal, circumoral, and circumanal hyperkeratotic plaques [1]. Since then, only three cases have been reported in the English literature [1-3].
Kahoru, Nishina   +4 more
exaly   +3 more sources

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