Results 91 to 100 of about 4,063 (129)
The Epidemiology and Treatment Outcomes of Facial Nerve Palsy Using a Population-Based Method. [PDF]
Ophthalmic Plast Reconstr SurgHwang CJ +3 more
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Differences in Cause-Specific Mortality in Patients With Rheumatoid Arthritis by Sex and Seropositivity. [PDF]
J RheumatolJoerns EK +7 more
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Proteolytic dysregulation in the skin: insight from rare monogenic skin diseases. [PDF]
Cell Tissue ResLi Z, Wang S, Blaydon DC, Kelsell DP.
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Journal of Cutaneous Pathology, 2001
Olmsted syndrome is an uncommon inherited disorder of keratinization that presents mutilating palmoplantar keratoderma, perioral hyperkeratosis, leukokeratosis and alopecia. We report a case of this rare syndrome diagnosed in a 48‐year‐old woman and confirms the existence of a generalized abnormality in keratin expression.
E, Fonseca +6 more
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Olmsted syndrome is an uncommon inherited disorder of keratinization that presents mutilating palmoplantar keratoderma, perioral hyperkeratosis, leukokeratosis and alopecia. We report a case of this rare syndrome diagnosed in a 48‐year‐old woman and confirms the existence of a generalized abnormality in keratin expression.
E, Fonseca +6 more
+7 more sources
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
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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
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Seminars in Dermatology, 1995
Nine cases of Olmsted syndrome have been reported in the world literature. In this syndrome, keratoderma usually starts during infancy on the palms and soles when the baby starts to use the feet for walking and the hands for grasping. Within weeks or months, there is progressive spread of solid, symmetrical, thick hyperkeratotic keratoderma to both ...
H O, Perry, W P, Su
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Nine cases of Olmsted syndrome have been reported in the world literature. In this syndrome, keratoderma usually starts during infancy on the palms and soles when the baby starts to use the feet for walking and the hands for grasping. Within weeks or months, there is progressive spread of solid, symmetrical, thick hyperkeratotic keratoderma to both ...
H O, Perry, W P, Su
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Semidominant Inheritance in Olmsted Syndrome [PDF]
Journal of Investigative Dermatology, 2016 Huijun Wang, Zhimiao Lin
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Olmsted syndrome with microtia
European Journal of Pediatric Dermatology, 2021Olmsted 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.
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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
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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
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Anesthetic management of a child with olmsted's syndrome
Journal of Anesthesia, 1994In 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 +2 more
exaly +3 more sources