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10.1590/abd1806-4841.20175211 http://scihub22266oqcxt.onion/10.1590/abd1806-4841.20175211 C5595615!5595615!28954117     free     free     free Deprecated: Implicit conversion from float 229.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       An+Bras+Dermatol 2017 ; 92 (4): 571-2 Nephropedia Template TP {{tp|p=28954117|t=2017. Do you know this syndrome? Heerfordt-Waldenström syndrome* |pdf=|usr=}}{{28954117}} gab.com Text Do you know this syndrome Heerfordt-Waldenström syndrome* JO: An Bras Dermatol http://www.kidney.de/pget.php?&tw=1&pmid=28954117 #FOAvip Heerfordt-Waldenström syndrome is a rare subacute variant of sarcoidosis, characterized by enlargement of the parotid or salivary glands, facial nerve paralysis and anterior uveitis. Granulomas with a peripheral lymphocyte deficit are found in the anatomic pathology of affected organs. It is normally self-limiting, with cure achieved between 12 and 36 months, but some prolonged cases have been reported. Diagnosis of the syndrome is clinical, and treatment depends on the degree of systemic impairment. Oral corticosteroids represent the first line treatment option. The mortality rate ranges between 1 and 5% of cases. Twit Text FOAVip Do you know this syndrome Heerfordt-Waldenström syndrome* ????An Bras Dermatol http://www.kidney.de/pget.php?&tw=1&pmid=28954117 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28954117 #FOAvip English Wikipedia <ref>{{Cite pmid|28954117}}</ref> Do you know this syndrome? Heerfordt-Waldenström syndrome* #MMPMID28954117 Fraga RC; Kakizaki P; Valente NYS; Portocarrero LKL; Teixeira MFS; Senise PF An Bras Dermatol 2017[Jul]; 92 (4): 571-2 PMID28954117show ga Heerfordt-Waldenström syndrome is a rare subacute variant of sarcoidosis, characterized by enlargement of the parotid or salivary glands, facial nerve paralysis and anterior uveitis. Granulomas with a peripheral lymphocyte deficit are found in the anatomic pathology of affected organs. It is normally self-limiting, with cure achieved between 12 and 36 months, but some prolonged cases have been reported. Diagnosis of the syndrome is clinical, and treatment depends on the degree of systemic impairment. Oral corticosteroids represent the first line treatment option. The mortality rate ranges between 1 and 5% of cases. äDo you know this syndrome? Heerfordt-Waldenström syndrome* (epmc).pdf DeepDyve Pubget Overpricing