About: Lamellar ichthyosis

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Lamellar ichthyosis, also known as ichthyosis lamellaris and nonbullous congenital ichthyosis, is a rare inherited skin disorder, affecting around 1 in 600,000 people.

Attributes	Values
rdf:type	Thing Disease yago:WikicatAutosomalRecessiveDisorders yago:WikicatCongenitalDisorders yago:Abnormality114501726 yago:Abstraction100002137 yago:Anomaly114505821 yago:Attribute100024264 yago:BirthDefect114465048 yago:Condition113920835 yago:Defect114464005 yago:Disease114070360 yago:Disorder114052403 yago:IllHealth114052046 yago:Illness114061805 yago:Imperfection114462666 yago:PathologicalState114051917 yago:PhysicalCondition114034177 disease yago:State100024720 umbel-rc:AilmentCondition
rdfs:label	سماك صفاحي (ar) Lamelläre Ichthyose (de) Lamellar ichthyosis (en) Ittiosi lamellare (it) Zespół dziecka kolodionowego (pl) Ламеллярный ихтиоз (ru) 層狀魚鱗癬 (zh)
rdfs:comment	السماك الصفاحي، ويسمي أيضا السماك الخلقي اللافقاعي، هو داءٌ جلديٌّ وراثيٌّ نادرٌ، يصيب نحو شخص من كل 600 ألف شخص. (ar) Lamellar ichthyosis, also known as ichthyosis lamellaris and nonbullous congenital ichthyosis, is a rare inherited skin disorder, affecting around 1 in 600,000 people. (en) Per ittiosi lamellare, nota anche con il termine ittiosi lamellare recessiva, in campo medico, si intende una patologia dermatologica, una condizione autosomica recessiva, la seconda forma di ittiosi più grave dopo l'ittiosi Arlecchino. (it) Zespół dziecka kolodionowego (ang. collodion baby) – opisowe określenie schorzeń z grupy rybiej łuski, objawiających się pokrywającą po urodzeniu ciało dziecka błoniastą warstwą, przywodzącą na myśl natłuszczony pergamin lub kolodium. (pl) Ламеллярный ихтиоз — врождённый небуллезный ихтиоз, наследуемый преимущественно по аутосомно-рецессивному типу, для которого , пластинчатый , эктропион.Впервые заболевание было описано в 1841 году Е. Селигманном. (ru) 層狀魚鱗癬 (自體隱性遺傳)是一種遺傳病，其會導致皮膚不良，角質會增厚及局部角化不全。皮膚亦因不正常的角質而缺乏防水功能。此遺傳病的發生率由500000至600000分之1。遺傳方面，其遺傳方式為體染色體隱性遺傳，不同研究得出不同發病基因。 (zh) Die Lamelläre Ichthyose (LI) ist die häufigste Form der autosomal-rezessiven kongenitalen Ichthyose und eine angeborene Erkrankung mit einer bereits bei Geburt bestehenden Schuppenbildung am ganzen Körper, aber ohne Erythrodermie. Mitunter werden unter der Bezeichnung „lamelläre Ichthyose“ mehrere genetisch heterogene Erkrankungen, auch eine autosomal-dominante Form, zusammengefasst. (de)
foaf:name	Ichthyosis lamellaris (en)
name	Ichthyosis lamellaris (en)
foaf:depiction
dcterms:subject	Autosomal recessive disorders Genodermatoses Rare diseases
Wikipage page ID	617547 (xsd:integer)
Wikipage revision ID	1048547032 (xsd:integer)
Link from a Wikipage to another Wikipage	Dehydration Hyperkeratosis Hypothermia Vaseline Genetics Neonatal intensive care unit Emollient Congenital hypothyroidism Consanguinity Autosomal recessive disorders Skin biopsy Collodion Ichthyosis Ichthyosis vulgaris dbr:Keratinocyte_transglutaminase Skin infection Autosomal recessive Trichothiodystrophy Acitretin Genodermatoses Rare diseases Harlequin type ichthyosis Ischemia Isotretinoin Aspirin ABCA12 Keratolytic Birth defect Blood test Ectropion Sjögren-Larsson syndrome Autosome Bullous congenital ichthyosiform erythroderma Newborn Recessive gene CYP4F22 Medicine Skin Netherton syndrome Palmoplantar keratoderma with anogenital leukokeratosis Salicylate intoxication Dorfman-Chanarin syndrome Gaucher disease Skin disease Congenital ichthyosiform erythrodema Conradi syndrome Ichthyosis variegata OMIM TGM1 dbr:Wikt:incubator dbr:Ketoadipiaciduria dbr:Koraxitrachitic_syndrome
sameAs	Lamellar ichthyosis Lamellar ichthyosis Lamellar ichthyosis Lamellar ichthyosis Lamellar ichthyosis

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