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10.4103/jomfp.JOMFP_170_16 http://scihub22266oqcxt.onion/10.4103/jomfp.JOMFP_170_16 C5596695!5596695!28932054     free     free     free       J+Oral+Maxillofac+Pathol 2017 ; 21 (2): 321 Nephropedia Template TP {{tp|p=28932054|t=2017. Darier disease: A rare genodermatosis |pdf=|usr=}}{{28932054}} gab.com Text Darier disease: A rare genodermatosis JO: J Oral Maxillofac Pathol http://www.kidney.de/pget.php?&tw=1&pmid=28932054 #FOAvip Darier disease (DD), also known as keratosis follicularis or dyskeratosis follicularis, is a rare autosomal dominant genodermatosis with high penetrance and variable expressivity. It is caused by mutations of ATP2A2 gene which encodes the sarco/endoplasmic reticulum Ca2+ ATPase isoform 2. It is clinically manifested by hyperkeratotic papules primarily affecting seborrheic areas on the head, neck and thorax, with less frequent involvement of the oral mucosa. When oral manifestations are present, they primarily affect the palatal and alveolar mucosa, are usually asymptomatic and are discovered in routine dental examination. Histologically, the lesions show suprabasal clefts with acantholytic and dyskeratotic cells. We present a case of 35-year-old female patient with typical clinical and histological features of DD. Twit Text FOAVip Darier disease: A rare genodermatosis ????J Oral Maxillofac Pathol http://www.kidney.de/pget.php?&tw=1&pmid=28932054 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28932054 #FOAvip English Wikipedia <ref>{{Cite pmid|28932054}}</ref> Darier disease: A rare genodermatosis #MMPMID28932054 Suryawanshi H; Dhobley A; Sharma A; Kumar P J Oral Maxillofac Pathol 2017[May]; 21 (2): 321 PMID28932054show ga Darier disease (DD), also known as keratosis follicularis or dyskeratosis follicularis, is a rare autosomal dominant genodermatosis with high penetrance and variable expressivity. It is caused by mutations of ATP2A2 gene which encodes the sarco/endoplasmic reticulum Ca2+ ATPase isoform 2. It is clinically manifested by hyperkeratotic papules primarily affecting seborrheic areas on the head, neck and thorax, with less frequent involvement of the oral mucosa. When oral manifestations are present, they primarily affect the palatal and alveolar mucosa, are usually asymptomatic and are discovered in routine dental examination. Histologically, the lesions show suprabasal clefts with acantholytic and dyskeratotic cells. We present a case of 35-year-old female patient with typical clinical and histological features of DD. äDarier disease: A rare genodermatosis (epmc).pdf DeepDyve Pubget Overpricing