{"id":108841,"date":"2021-05-27T09:28:00","date_gmt":"2021-05-27T09:28:00","guid":{"rendered":"https:\/\/www.healthbenefitstimes.com\/glossary\/?p=108841"},"modified":"2021-05-27T09:28:00","modified_gmt":"2021-05-27T09:28:00","slug":"infantile-hypercalcemia","status":"publish","type":"post","link":"https:\/\/www.healthbenefitstimes.com\/glossary\/infantile-hypercalcemia\/","title":{"rendered":"Infantile hypercalcemia"},"content":{"rendered":"<p>Infantile hypercalcemia, or Williams syndrome, is a congenital disorder that affects a child\u2019s cognitive, physical, and behavioral development. It has been linked to the absence of genetic material on Chromosome 7. The deletion of portions of this chromosome, where elastin is made, results in many of the physical features seen in Williams syndrome.<\/p>\n<hr \/>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Infantile hypercalcemia, or Williams syndrome, is a congenital disorder that affects a child\u2019s cognitive, physical, and behavioral development. It has been linked to the absence of genetic material on Chromosome 7. The deletion of portions of this chromosome, where elastin is made, results in many of the physical features seen in Williams syndrome. &nbsp;<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[9],"tags":[],"class_list":["post-108841","post","type-post","status-publish","format-standard","hentry","category-i"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v21.1 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Infantile hypercalcemia - Definition of Infantile hypercalcemia<\/title>\n<meta name=\"description\" content=\"Infantile hypercalcemia, or Williams syndrome, is a congenital disorder that affects a child\u2019s cognitive, physical, and behavioral development. It has been linked to the absence of genetic material on Chromosome 7. The deletion of portions of this chromosome, where elastin is made, results in many of the physical features seen in Williams syndrome.\" \/>\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\/infantile-hypercalcemia\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Infantile hypercalcemia - Definition of Infantile hypercalcemia\" \/>\n<meta property=\"og:description\" content=\"Infantile hypercalcemia, or Williams syndrome, is a congenital disorder that affects a child\u2019s cognitive, physical, and behavioral development. It has been linked to the absence of genetic material on Chromosome 7. 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