Ichthyosis

  • 41ichthyosis hystrix — [L. hysґtrix porcupine] any of several rare autosomal dominant skin disorders in which large areas of the skin have wartlike growths that are sometimes pointed to resemble porcupine quills; some types are severe forms of epidermolytic… …

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  • 42ichthyosis palmaris et plantaris — palmoplantar keratoderma …

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  • 43ichthyosis uteri — a condition marked by transformation of the columnar epithelium of the endometrium into stratified squamous epithelium …

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  • 44X-linked ichthyosis — Infobox Disease Name = X linked ichthyosis Caption = DiseasesDB = 29136 ICD10 = ICD10|Q|80|1|q|80 ICD9 = ICD9|757.1 ICDO = OMIM = 308100 MedlinePlus = eMedicineSubj = derm eMedicineTopic = 191 MeshID = D016114 X linked ichthyosis (XLI) is a skin… …

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  • 45Harlequin type ichthyosis — Infobox Disease Name = Harlequin type ichthyosis Caption = Lithographic depiction of a fetus affected by harlequin ichthyosis DiseasesDB = 30052 ICD10 = ICD10|Q|80|4|q|80 ICD9 = ICD9|757.1 ICDO = OMIM = 242500 |vsnfy,gkmfnbdbnhdmfyjhrythtyjruythe …

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  • 46Keratitis-Ichthyosis-Taubheitssyndrom — Klassifikation nach ICD 10 H90.5 Hörverlust durch Schallempfindungsstörung, nicht näher bezeichnet Angeborene Schwerhörigkeit oder Taubheit o. n. A. Q80.8 Sonsti …

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  • 47lamellar ichthyosis — n a rare inherited form of ichthyosis characterized by large coarse scales * * * ichthyosis lamellaris a genetically and clinically heterogeneous, autosomal recessive form of ichthyosis, in which the affected infant is born encased in a… …

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  • 48Neonatal ichthyosis–sclerosing cholangitis syndrome — Classification and external resources OMIM 607626 Neonatal ichthyosis–sclerosing cholangitis syndrome (also known as NISCH syndrome [1] and Ichthyosis–sclerosing cholangitis syndrome …

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  • 49Keratitis-Ichthyosis-Deafness — Klassifikation nach ICD 10 H90.5 Hörverlust durch Schallempfindungsstörung, nicht näher bezeichnet Angeborene Schwerhörigkeit oder Taubheit o. n. A. Q80.8 Sonstige Ichthyosis congenita …

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  • 50Keratitis-ichthyosis-deafness syndrome — An inherited disorder in which affected persons have: {{}}Keratitis gradual destruction of the cornea of the eye, sometimes leading to blindness Ichthyosis localized areas of disfiguring reddish thickened skin ( fish skin ) Deafness at birth… …

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