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10.1155/2015/321291 http://scihub22266oqcxt.onion/10.1155/2015/321291 C4588317!4588317!26451367     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       Biomed+Res+Int 2015 ; 2015 (ä): ä Nephropedia Template TP {{tp|p=26451367|t=2015. The Genetics and the Genomics of Primary Congenital Glaucoma |pdf=|usr=}}{{26451367}} gab.com Text The Genetics and the Genomics of Primary Congenital Glaucoma JO: Biomed Res Int http://www.kidney.de/pget.php?&tw=1&pmid=26451367 #FOAvip The sight is one of the five senses allowing an autonomous and high-quality life, so that alterations of any ocular component may result in several clinical phenotypes (from conjunctivitis to severe vision loss and irreversible blindness). Most parts of clinical phenotypes have been significantly associated with mutations in genes regulating the normal formation and maturation of the anterior segments of the eye. Among the eye anterior segment disorders, special attention is given to Glaucoma as it represents one of the major causes of bilateral blindness in the world, with an onset due to Mendelian or multifactorial genetic-causative traits. This review will point out the attention on the Primary Congenital Glaucoma (PCG), which is usually transmitted according to an autosomal-recessive inheritance pattern. Taking into consideration the genetic component of the PCG, it is possible to observe a strong heterogeneity concerning the disease-associated loci (GLC3), penetrance defects, and expressivity of the disease. Given the strong PGC heterogeneity, pre- and posttest genetic counseling plays an essential role in the achievement of an appropriate management of PCG, in terms of medical, social, and psychological impact of the disease. Twit Text FOAVip The Genetics and the Genomics of Primary Congenital Glaucoma ????Biomed Res Int http://www.kidney.de/pget.php?&tw=1&pmid=26451367 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26451367 #FOAvip English Wikipedia <ref>{{Cite pmid|26451367}}</ref> The Genetics and the Genomics of Primary Congenital Glaucoma #MMPMID26451367 Cascella R; Strafella C; Germani C; Novelli G; Ricci F; Zampatti S; Giardina E Biomed Res Int 2015[]; 2015 (ä): ä PMID26451367show ga The sight is one of the five senses allowing an autonomous and high-quality life, so that alterations of any ocular component may result in several clinical phenotypes (from conjunctivitis to severe vision loss and irreversible blindness). Most parts of clinical phenotypes have been significantly associated with mutations in genes regulating the normal formation and maturation of the anterior segments of the eye. Among the eye anterior segment disorders, special attention is given to Glaucoma as it represents one of the major causes of bilateral blindness in the world, with an onset due to Mendelian or multifactorial genetic-causative traits. This review will point out the attention on the Primary Congenital Glaucoma (PCG), which is usually transmitted according to an autosomal-recessive inheritance pattern. Taking into consideration the genetic component of the PCG, it is possible to observe a strong heterogeneity concerning the disease-associated loci (GLC3), penetrance defects, and expressivity of the disease. Given the strong PGC heterogeneity, pre- and posttest genetic counseling plays an essential role in the achievement of an appropriate management of PCG, in terms of medical, social, and psychological impact of the disease. äThe Genetics and the Genomics of Primary Congenital Glaucoma (epmc).pdf DeepDyve Pubget Overpricing