Kindler Syndrome: A case Report from Iran

• Päätekijät: Maryam Amirchaghmaghi (Tekijä), Amir Moeintaghavi (Tekijä), Javid Rasekhi (Tekijä), Pegah Mosannen Mozafari (Tekijä), Zohreh Dalirsani (Tekijä), Amir Hossein Jafarian Jafarian (Tekijä)
• Aineistotyyppi: Kirja
• Julkaistu: Mashhad University of Medical Sciences, 2014-06-01T00:00:00Z.
• Aiheet: article
• Linkit: Connect to this object online.

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....