Ichthyosis
121Keratinocyte transglutaminase — Transglutaminase 1 (K polypeptide epidermal type I, protein glutamine gamma glutamyltransferase), also known as TGM1, is a human gene.cite web | title = Entrez Gene: TGM1 transglutaminase 1 (K polypeptide epidermal type I, protein glutamine gamma …
122КЕРАТОЗЫ — (keratosis, keratoma, kera todermia, keratodermatosis) (от греч. keras рог), сборное понятие для целого ряда кожных заболеваний невоспалительного происхождения, к рые морфологически и па толого анатомически характеризуются умеренным утолщением… …
123Isotretinoin — Systematic (IUPAC) name (13cis) …
124Collodion baby — Infobox Disease Name = Collodion baby Caption = DiseasesDB = 30052 OMIM = 242300 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = In medicine, the term collodion baby applies to newborns who appear to have an extra layer of skin that has a …
125Ichtyose — (du grec ichthyos = poisson) est le nom d une famille de maladies congénitales de la peau. L ichtyose est une dystrophie cutanée congénitale qui correspond à un état particulier de la peau, sèche et couverte de squames fines à bords libres… …
126Cystic fibrosis — Classification and external resources A breathing treatment for cystic fibrosis, using a mask nebuliser and a ThAIRapy Vest ICD 10 E …
127Tay syndrome — Infobox Disease Name = Tay syndrome Caption = DiseasesDB = 13341 ICD10 = ICD9 = ICDO = OMIM = 601675 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Tay syndrome is a recessive hereditary disease characterised by trichothiodystrophy… …
128Fischschuppenkrankheit — (Ichthyosis), auf Verdickung und Härte des Papillarkörpers der Lederhaut, vermehrter Bildung und rascher Verhornung der Epidermiszellen beruhende Hautkrankheit. Es bilden sich trockne, hornartige, in kleine Abschnitte zerspringende… …
