{"id":108811,"date":"2021-05-27T08:21:24","date_gmt":"2021-05-27T08:21:24","guid":{"rendered":"https:\/\/www.healthbenefitstimes.com\/glossary\/?p=108811"},"modified":"2021-05-27T08:21:24","modified_gmt":"2021-05-27T08:21:24","slug":"ichthyosis-congenita","status":"publish","type":"post","link":"https:\/\/www.healthbenefitstimes.com\/glossary\/ichthyosis-congenita\/","title":{"rendered":"Ichthyosis congenita"},"content":{"rendered":"<p>Ichthyosis congenita is an inherited skin disorder characterized by generalized dry and rough skin. All babies who suffer from an autosomal recessive congenita ichthyosis are collodion babies at birth. Collodion babies are born with a translucent or opaque membrane that covers the entire body and lasts for days to weeks. Congenita ichthyosis presents on a spectrum in which lamellar ichthyosis is the most severe and non bullous congenital ichthyosis is a mild form of congenita ichthyosis. In lamellar ichthyosis the collodion membrane is replaced by dark brown plate like scales without erythroderma (abnormal redness of the skin). The non bullous type presents with erythroderma with fine white scales.<\/p>\n<hr \/>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Ichthyosis congenita is an inherited skin disorder characterized by generalized dry and rough skin. All babies who suffer from an autosomal recessive congenita ichthyosis are collodion babies at birth. Collodion babies are born with a translucent or opaque membrane that covers the entire body and lasts for days to weeks. Congenita ichthyosis presents on a [&hellip;]<\/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-108811","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>Ichthyosis congenita - Definition of Ichthyosis congenita<\/title>\n<meta name=\"description\" content=\"Ichthyosis congenita is an inherited skin disorder characterized by generalized dry and rough skin. All babies who suffer from an autosomal recessive congenita ichthyosis are collodion babies at birth. Collodion babies are born with a translucent or opaque membrane that covers the entire body and lasts for days to weeks. Congenita ichthyosis presents on a spectrum in which lamellar ichthyosis is the most severe and non bullous congenital ichthyosis is a mild form of congenita ichthyosis. In lamellar ichthyosis the collodion membrane is replaced by dark brown plate like scales without erythroderma (abnormal redness of the skin). The non bullous type presents with erythroderma with fine white scales.\" \/>\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\/ichthyosis-congenita\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Ichthyosis congenita - Definition of Ichthyosis congenita\" \/>\n<meta property=\"og:description\" content=\"Ichthyosis congenita is an inherited skin disorder characterized by generalized dry and rough skin. All babies who suffer from an autosomal recessive congenita ichthyosis are collodion babies at birth. Collodion babies are born with a translucent or opaque membrane that covers the entire body and lasts for days to weeks. Congenita ichthyosis presents on a spectrum in which lamellar ichthyosis is the most severe and non bullous congenital ichthyosis is a mild form of congenita ichthyosis. In lamellar ichthyosis the collodion membrane is replaced by dark brown plate like scales without erythroderma (abnormal redness of the skin). The non bullous type presents with erythroderma with fine white scales.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.healthbenefitstimes.com\/glossary\/ichthyosis-congenita\/\" \/>\n<meta property=\"og:site_name\" content=\"Glossary\" \/>\n<meta property=\"article:published_time\" content=\"2021-05-27T08:21:24+00:00\" \/>\n<meta name=\"author\" content=\"Glossary\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Glossary\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"1 minute\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/ichthyosis-congenita\/\",\"url\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/ichthyosis-congenita\/\",\"name\":\"Ichthyosis congenita - Definition of Ichthyosis congenita\",\"isPartOf\":{\"@id\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/#website\"},\"datePublished\":\"2021-05-27T08:21:24+00:00\",\"dateModified\":\"2021-05-27T08:21:24+00:00\",\"author\":{\"@id\":\"https:\/\/www.healthbenefitstimes.com\/glossary\/#\/schema\/person\/ccfef987a4882e6356ae6d77d33e74c5\"},\"description\":\"Ichthyosis congenita is an inherited skin disorder characterized by generalized dry and rough skin. All babies who suffer from an autosomal recessive congenita ichthyosis are collodion babies at birth. Collodion babies are born with a translucent or opaque membrane that covers the entire body and lasts for days to weeks. Congenita ichthyosis presents on a spectrum in which lamellar ichthyosis is the most severe and non bullous congenital ichthyosis is a mild form of congenita ichthyosis. In lamellar ichthyosis the collodion membrane is replaced by dark brown plate like scales without erythroderma (abnormal redness of the skin). 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All babies who suffer from an autosomal recessive congenita ichthyosis are collodion babies at birth. Collodion babies are born with a translucent or opaque membrane that covers the entire body and lasts for days to weeks. Congenita ichthyosis presents on a spectrum in which lamellar ichthyosis is the most severe and non bullous congenital ichthyosis is a mild form of congenita ichthyosis. In lamellar ichthyosis the collodion membrane is replaced by dark brown plate like scales without erythroderma (abnormal redness of the skin). 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All babies who suffer from an autosomal recessive congenita ichthyosis are collodion babies at birth. Collodion babies are born with a translucent or opaque membrane that covers the entire body and lasts for days to weeks. Congenita ichthyosis presents on a spectrum in which lamellar ichthyosis is the most severe and non bullous congenital ichthyosis is a mild form of congenita ichthyosis. In lamellar ichthyosis the collodion membrane is replaced by dark brown plate like scales without erythroderma (abnormal redness of the skin). 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