WebMembers of the medical team for Dyschromatosis symmetrica hereditaria 1 may include: Primary care provider (PCP) A primary care provider (PCP) serves as the first line of care. PCPs diagnose and treat common conditions, manage a patient’s overall health, and provide referrals to specialists. Types of PCPs include doctors practicing general ... http://article.sapub.org/10.5923.j.health.20240701.02.html

Clinical and Genetic Review of Hereditary Acral Reticulate ... - Hindawi

WebDyschromatosis symmetrica hereditaria (DSH) is a rare pigmentary genodermatosis, which is acquired by autosomal dominant inheritance with high penetrance. Most … WebFeb 18, 2016 · Dyschromatosis symmetrica hereditaria (DSH) is a rare autosomal dominant cutaneous disorder caused by the mutations of adenosine deaminase acting on RNA1 (ADAR1) gene. We present a clinical and genetic study of seven unrelated families and two sporadic cases with DSH for mutations in the full coding sequence of ADAR1 … rawls political liberalism

Orphanet: Dyschromatosis symmetrica hereditaria

WebMay 1, 2003 · Dyschromatosis symmetrica hereditaria (DSH) (OMIM 127400) is also called reticulate acropigmentation of Dohi and symmetric dyschromatosis of the … WebNov 7, 2014 · Dyschromatosis symmetrica hereditaria (DSH) is a pigmentary genodermatosis of autosomal dominant inheritance caused by a mutation of adenosine deaminase acting on the RNA 1 gene (ADAR1). It is ... WebSep 16, 2016 · To the Editor: Dyschromatosis symmetrica hereditaria (DSH)(Online Mendelian Inheritance in Man 127400), also called reticulate acropigmentation of Dohi, is … simple hills