性连锁鱼鳞病(X-Linked ichthyosis)又称黑鱼鳞病。[病因与发病机制]本病与类固醇硫酸酯酶异常有关,类固醇硫酸酯酶水解硫酸 … www.jsyulb.com|基于35个网页 2. X-性联遗传鱼鳞癣 ... Q800 Ichthyosis vulgaris 寻常鱼鳞癣 Q801X-linked ichthyosisX-性联遗传鱼鳞癣Q802 Lamellar ichthyosis 层状鱼鳞癣 ......
Ichthyosis nigricans Definition Hereditary disorder of keratinization, characterized by severe scaling, especially on the extremitiesPathogenesis X-linked trait; caused by a steroid sulfatase deficiency resulting from abnormalities in its coding gene (STS); retention hyperkeratosis from delayed dissolution of ...
X-linked ichthyosis: an update. Br J Dermatol. 1999; 141 :617–27. [ PubMed ]Herndndez-Martin A, Gonzdlez-Sarmiento R, De Unamuno P. X-linked ichthyosis: an update[J].Br J Dermatol, 1999,141 (4) :617-627.Hernandez-Martin, A., Gonzalez-Sarmiento, R., and De Unamuno, P. ...
1) X-linked ichthyosis X-性联鱼鳞病 1. Objective To identify the mutation genes of paitents and their families with ichthyosis vulgaris;X-linked ichthyosis;lamellar ichthyosis;epidermolytic hyperkeratosis ichthyosis and to analyse the possible correlations between genotype and phenotype. ...
There is fine scaling X-Linked Ichthyosis This is also has a very early onset, at birth or within the first 3 months of age. The distribution of scaling differs substantially from ichthyosis vulgaris. Thus it involves the scalp, ears, neck, and flexures and affects the abdomen and the ...
(redirected fromX-linked ichthyosis) Thesaurus Medical Acronyms Encyclopedia Wikipedia Related to X-linked ichthyosis:lamellar ichthyosis ich·thy·o·sis (ĭk′thē-ō′sĭs) n. Any of a group of chiefly genetic disorders that are characterized by dry, scaly, and often thickened skin. ...
1)X-linked ichthyosisX-性联鱼鳞病 1.Objective To identify the mutation genes of paitents and their families with ichthyosis vulgaris;X-linked ichthyosis;lamellar ichthyosis;epidermolytic hyperkeratosis ichthyosis and to analyse the possible correlations between genotype and phenotype.③X-性联鱼鳞病患者...
2)X-linked ichthyosis (XLI)X连锁鳞癣 3)X-linked ichthyosisX-性联鱼鳞病 1.Objective To identify the mutation genes of paitents and their families with ichthyosis vulgaris;X-linked ichthyosis;lamellar ichthyosis;epidermolytic hyperkeratosis ichthyosis and to analyse the possible correlations between gen...
Regional assignment of the steroid sulfatase--X-linked ichthyosis locus: Implications for a noninactivated region on the short arm of human X chromosome Patients with recessive X-linked ichthyosis, one of the inherited types of excessive stratum corneum cohesion, have deficient steroid sulfatase in fi...
Recessive X-linked Ichthyosis Recessive X-linkedichthyosis(RXLI) is an uncommon condition, affecting 1 in 6000 males. Signs of the disorder are present at birth in one fifth of affected infants; 85% develop skin changes by 3 months of age. The characteristic cutaneous finding is coarse, browni...