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10.1038/ejhg.2015.41 http://scihub22266oqcxt.onion/10.1038/ejhg.2015.41 C4486366!4486366!25804399     free     free     free Deprecated: Implicit conversion from float 227.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 227.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 227.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 227.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 227.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 227.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 227.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\25804399.jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Eur+J+Hum+Genet 2015 ; 23 (12): 1634-9 Nephropedia Template TP {{tp|p=25804399|t=2015. The lymphatic phenotype in Turner syndrome: an evaluation of nineteen patients and literature review |pdf=|usr=}}{{25804399}} gab.com Text The lymphatic phenotype in Turner syndrome: an evaluation of nineteen patients and literature review JO: Eur J Hum Genet http://www.kidney.de/pget.php?&tw=1&pmid=25804399 #FOAvip Turner syndrome is a complex disorder caused by an absent or abnormal sex chromosome. It affects 1/2000?1/3000 live-born females. Congenital lymphoedema of the hands, feet and neck region (present in over 60% of patients) is a common and key diagnostic indicator, although is poorly described in the literature. The aim of this study was to analyse the medical records of a cohort of 19 Turner syndrome patients attending three specialist primary lymphoedema clinics, to elucidate the key features of the lymphatic phenotype and provide vital insights into its diagnosis, natural history and management. The majority of patients presented at birth with four-limb lymphoedema, which often resolved in early childhood, but frequently recurred in later life. The swelling was confined to the legs and hands with no facial or genital swelling. There was only one case of suspected systemic involvement (intestinal lymphangiectasia). The lymphoscintigraphy results suggest that the lymphatic phenotype of Turner syndrome may be due to a failure of initial lymphatic (capillary) function. Twit Text FOAVip The lymphatic phenotype in Turner syndrome: an evaluation of nineteen patients and literature review ????Eur J Hum Genet http://www.kidney.de/pget.php?&tw=1&pmid=25804399 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=25804399 #FOAvip English Wikipedia <ref>{{Cite pmid|25804399}}</ref> The lymphatic phenotype in Turner syndrome: an evaluation of nineteen patients and literature review #MMPMID25804399 Atton G; Gordon K; Brice G; Keeley V; Riches K; Ostergaard P; Mortimer P; Mansour S Eur J Hum Genet 2015[Dec]; 23 (12): 1634-9 PMID25804399show ga Turner syndrome is a complex disorder caused by an absent or abnormal sex chromosome. It affects 1/2000?1/3000 live-born females. Congenital lymphoedema of the hands, feet and neck region (present in over 60% of patients) is a common and key diagnostic indicator, although is poorly described in the literature. The aim of this study was to analyse the medical records of a cohort of 19 Turner syndrome patients attending three specialist primary lymphoedema clinics, to elucidate the key features of the lymphatic phenotype and provide vital insights into its diagnosis, natural history and management. The majority of patients presented at birth with four-limb lymphoedema, which often resolved in early childhood, but frequently recurred in later life. The swelling was confined to the legs and hands with no facial or genital swelling. There was only one case of suspected systemic involvement (intestinal lymphangiectasia). The lymphoscintigraphy results suggest that the lymphatic phenotype of Turner syndrome may be due to a failure of initial lymphatic (capillary) function. äThe lymphatic phenotype in Turner syndrome: an evaluation of nineteen (epmc).pdf DeepDyve Pubget Overpricing