Olmsted syndrome is a rare disorder characterized by the combination of periorificial, keratotic plaques and bilateral palmoplantar keratoderma. New associated features are being reported. Olmsted syndrome is particularly rare in a female patient, and we report such a case in a six year-old Indian girl, who presented with keratoderma of her soles since birth and on her palms since the age of two years along with perioral and perinasal hyperkeratosis. She had sparse, light brown, thin hair. Although the psychomotor development of the child was normal until 18 months of age, the keratoderma plaques had restricted the child′s mobility after that stage
Pachyonychia congenita (PC) is a rare, usually autosomal dominant, genodermatosis characterized by t...
Purpose: To present the ophthalmic manifestations of a 3-month old female with SCALP syndrome. Obser...
Introduction: Olmsted syndrome (OS) is a rare congenital skin disorder presenting with a combination...
Olmsted syndrome is a rare congenital, sharply circumscribed transgredient palmoplantar keratoderma....
Olmsted syndrome is a rare congenital entity characterized by combination of symmetrical, sharply-de...
Olmsted syndrome (OS) is a rare congenital, sharply circumscribed transgredient palmoplantar keratod...
Olmsted syndrome (OS) is a rare congenital skin disorder characterized by palmoplantar keratoderma, ...
The inheritance of Olmsted syndrome that is a very rare con-genital with transgredient palmoplantar ...
Olmsted syndrome (OS) is a rare congenital skin disorder characterized by severe palmoplantar and pe...
We report a case of mutilating keratoderma with alopecia and keratoses follicularis spinulosa decalv...
BACKGROUND: Olmsted syndrome is a rare congenital skin disorder presenting with periorifical hyperke...
BACKGROUND: Olmsted syndrome is a rare congenital skin disorder presenting with periorifical hyperke...
IMPORTANCE: Olmsted syndrome (OS) is a rare keratinizing disorder characterized by excessive epiderm...
Keratitis-Icthyosis-Deafness syndrome is a rare congenital disorder characterized by keratitis, icht...
The Huriez syndrome is a rare autosomal dominant transgradient palmoplantar keratoderma which is cha...
Pachyonychia congenita (PC) is a rare, usually autosomal dominant, genodermatosis characterized by t...
Purpose: To present the ophthalmic manifestations of a 3-month old female with SCALP syndrome. Obser...
Introduction: Olmsted syndrome (OS) is a rare congenital skin disorder presenting with a combination...
Olmsted syndrome is a rare congenital, sharply circumscribed transgredient palmoplantar keratoderma....
Olmsted syndrome is a rare congenital entity characterized by combination of symmetrical, sharply-de...
Olmsted syndrome (OS) is a rare congenital, sharply circumscribed transgredient palmoplantar keratod...
Olmsted syndrome (OS) is a rare congenital skin disorder characterized by palmoplantar keratoderma, ...
The inheritance of Olmsted syndrome that is a very rare con-genital with transgredient palmoplantar ...
Olmsted syndrome (OS) is a rare congenital skin disorder characterized by severe palmoplantar and pe...
We report a case of mutilating keratoderma with alopecia and keratoses follicularis spinulosa decalv...
BACKGROUND: Olmsted syndrome is a rare congenital skin disorder presenting with periorifical hyperke...
BACKGROUND: Olmsted syndrome is a rare congenital skin disorder presenting with periorifical hyperke...
IMPORTANCE: Olmsted syndrome (OS) is a rare keratinizing disorder characterized by excessive epiderm...
Keratitis-Icthyosis-Deafness syndrome is a rare congenital disorder characterized by keratitis, icht...
The Huriez syndrome is a rare autosomal dominant transgradient palmoplantar keratoderma which is cha...
Pachyonychia congenita (PC) is a rare, usually autosomal dominant, genodermatosis characterized by t...
Purpose: To present the ophthalmic manifestations of a 3-month old female with SCALP syndrome. Obser...
Introduction: Olmsted syndrome (OS) is a rare congenital skin disorder presenting with a combination...