منابع مشابه
Netherton syndrome: report of two cases
Netherton syndrome is a rare autosomal recessive condition with variable expression. It comprises an ichthyosiform dermatitis and erythroderma of variable intensity associated with hair abnormalities and features of atopy. The pathognomic (required for diagnosis) feature is trichorrhexis invaginata identified by microscopic examination of hair shaft. Ichthyosis linearis circumflexa is ano...
متن کاملReport of a Case Report of Kindler Syndrome
A 13 years old boy with progressive poikiloderma, bullous lesions in the extremities and photosensitivity is reported. Physical examinations were otherwise normal, his physical development was normal, no other family member had a similar disease. Routin laboratory exams were in the normal limits.Histopathology exams from poikilodermatous skin showed atrophy of the epidermis, liquification degen...
متن کاملWilson Mikity Syndrome (WMS): Report of Two Cases
Deux cas de Syndr'.:lme de Wilson-Mikity sont rapportes: le premier c:mcerne un premature chez qui les signes d'insuffisance re:,piratoire ont debutes tro;s semaines apres !a naissance. La radiographie a mis en evidenc Le deuxieme malade i:-ernit 2.EO::J kilos lors de son hospitalisati::>n a l'ag:c d qu·11,c jous. La radiograp'.1ie pulmonaire mett en ev;dencde:, opacite rec!iculaires bilatera...
متن کاملKindler Syndrome: A case Report from Iran
Kindler syndrome (KS) is a rare, autosomal recessive genodermatosis characterized by skin blistering and photosensitivity in infancy, progressive poikiloderma, and diffuse cutaneous atrophy. It affects the skin, mucous membranes, and oral cavity and is caused by mutations in the KIND1 gene on 20p12.3. The first case of KS associated with periodontitis was reported in 1996, and have been infrequ...
متن کاملKindler syndrome.
Kindler syndrome is a rare autosomal recessive disorder associated with skin fragility. It is characterized by blistering in infancy, photosensitivity and progressive poikiloderma. The syndrome involves the skin and mucous membrane with radiological changes. The genetic defect has been identified on the short arm of chromosome 20. This report describes an 18-year-old patient with classical feat...
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ژورنال
عنوان ژورنال: Anais Brasileiros de Dermatologia
سال: 2012
ISSN: 0365-0596
DOI: 10.1590/s0365-05962012000500020