The Stiff Skin Syndrome

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Stiff skin syndrome - Case report Síndrome stiff skin - Relato de caso

Stiff skin syndrome is a rare scleroderma-like disorder of unknown etiology characterized by stone-hard indurations of skin, mild hypertrichosis and limited joint mobility. No effective treatment has yet been found. Exercises and rehabilitative therapy are important in maintaining the patient's quality of life. The authors present a case of a two-year-old boy with progressive skin hardening sin...

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The stiff skin syndrome: case series, differential diagnosis of the stiff skin phenotype, and review of the literature.

BACKGROUND Stiff skin syndrome is a sclerodermalike disorder that presents in infancy or early childhood with rock-hard skin, limited joint mobility, and mild hypertrichosis in the absence of visceral or muscle involvement, immunologic abnormalities, or vascular hyperreactivity. OBSERVATIONS We describe 6 children who fit criteria for stiff skin syndrome. A review of the clinical range of thi...

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Congenital fascial dystrophy or stiff skin syndrome: a case report.

1. Kanitakis J, Lora V. Pagetoid dyskeratosis: A frequent pitfall in dermatopathology. Eur J Dermatol. 2010;20:123--4. 2. Toyonaga E, Inokuma D, Abe Y, Abe R, Shimizu H. Pagetoid dyskeratosis with parallel ridge pattern under dermoscopy. JAMA Dermatol. 2013;149:109--11. 3. Frenk E, Delacrétraz J. Hydropic degeneration of epidermal keratinocytes. An alteration leading to patchy hyperpigmentation...

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Congenital Fascial Dystrophy or Stiff Skin Syndrome: A Case Report

1. Kanitakis J, Lora V. Pagetoid dyskeratosis: A frequent pitfall in dermatopathology. Eur J Dermatol. 2010;20:123--4. 2. Toyonaga E, Inokuma D, Abe Y, Abe R, Shimizu H. Pagetoid dyskeratosis with parallel ridge pattern under dermoscopy. JAMA Dermatol. 2013;149:109--11. 3. Frenk E, Delacrétraz J. Hydropic degeneration of epidermal keratinocytes. An alteration leading to patchy hyperpigmentation...

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Stiff skin syndrome: evidence for an inflammation-independent fibrosis?

OBJECTIVES Stiff skin syndrome (SSS) is a rare scleroderma-like syndrome of unknown aetiology. A 16-year-old boy presented with thoracic and abdominal asymmetry, and 'orange peel' cutaneous lesions, with fibrotic stone-hard indurations at the buttocks, thighs and arms leading to secondary joint contractures of the extremities. Our aim was to analyse the expression of extracellular matrix (ECM) ...

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ژورنال

عنوان ژورنال: Archives of Dermatology

سال: 2008

ISSN: 0003-987X

DOI: 10.1001/archderm.144.10.1351