{"id":11611,"date":"2020-03-03T10:12:35","date_gmt":"2020-03-03T10:12:35","guid":{"rendered":"https:\/\/www.healthbenefitstimes.com\/glossary\/?p=11611"},"modified":"2023-08-18T06:35:38","modified_gmt":"2023-08-18T06:35:38","slug":"piebaldism","status":"publish","type":"post","link":"https:\/\/www.healthbenefitstimes.com\/glossary\/piebaldism\/","title":{"rendered":"Piebaldism"},"content":{"rendered":"<p><a href=\"https:\/\/www.healthbenefitstimes.com\/glossary\/wp-content\/uploads\/2020\/03\/Piebaldism.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-thumbnail wp-image-11612\" src=\"https:\/\/www.healthbenefitstimes.com\/glossary\/wp-content\/uploads\/2020\/03\/Piebaldism-150x150.jpg\" alt=\"\" width=\"150\" height=\"150\" srcset=\"https:\/\/www.healthbenefitstimes.com\/glossary\/wp-content\/uploads\/2020\/03\/Piebaldism-150x150.jpg 150w, https:\/\/www.healthbenefitstimes.com\/glossary\/wp-content\/uploads\/2020\/03\/Piebaldism-384x386.jpg 384w\" sizes=\"auto, (max-width: 150px) 100vw, 150px\" \/><\/a>Rare autosomal dominant disorder of melanocyte development characterized by distinct patches of skin and hair that contain no pigment.<\/p>\n<hr \/>\n<div class=\"group w-full text-token-text-primary border-b border-black\/10 dark:border-gray-900\/50 bg-gray-50 dark:bg-[#444654]\">\n<div class=\"flex p-4 gap-4 text-base md:gap-6 md:max-w-2xl lg:max-w-[38rem] xl:max-w-3xl md:py-6 lg:px-0 m-auto\">\n<div class=\"relative flex w-[calc(100%-50px)] flex-col gap-1 md:gap-3 lg:w-[calc(100%-115px)]\">\n<div class=\"flex flex-grow flex-col gap-3\">\n<div class=\"min-h-[20px] flex flex-col items-start gap-3 overflow-x-auto whitespace-pre-wrap break-words\">\n<div class=\"markdown prose w-full break-words dark:prose-invert light AIPRM__conversation__response\">\n<p>An infrequent genetic condition where uneven patches of missing dark pigment melanin lead to depigmented sections of skin and, at times, hair. Frequently, a white segment appears at the center of the face, which can encompass the hair, eyebrows, and skin. Piebaldism exhibits inheritance through an autosomal dominant pattern.<\/p>\n<hr \/>\n<p>&nbsp;<\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>Rare autosomal dominant disorder of melanocyte development characterized by distinct patches of skin and hair that contain no pigment. An infrequent genetic condition where uneven patches of missing dark pigment melanin lead to depigmented sections of skin and, at times, hair. Frequently, a white segment appears at the center of the face, which can encompass [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":11612,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[16],"tags":[],"class_list":["post-11611","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-p"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v21.1 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Piebaldism - Definition of Piebaldism<\/title>\n<meta name=\"description\" content=\"Rare autosomal dominant disorder of melanocyte development characterized by distinct patches of skin and hair that contain no pigment.An infrequent genetic condition where uneven patches of missing dark pigment melanin lead to depigmented sections of skin and, at times, hair. Frequently, a white segment appears at the center of the face, which can encompass the hair, eyebrows, and skin. Piebaldism exhibits inheritance through an autosomal dominant pattern.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.healthbenefitstimes.com\/glossary\/piebaldism\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Piebaldism - Definition of Piebaldism\" \/>\n<meta property=\"og:description\" content=\"Rare autosomal dominant disorder of melanocyte development characterized by distinct patches of skin and hair that contain no pigment.An infrequent genetic condition where uneven patches of missing dark pigment melanin lead to depigmented sections of skin and, at times, hair. 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