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・ X-Ray Specs
・ X-Ray Specs (comic strip)
・ X-Ray Specs (novelty)
・ X-Ray Spectrometry (journal)
・ X-ray spectroscopy
・ X-Ray Spex
・ X-ray standing waves
・ X-ray star
・ X-ray telescope
・ X-ray transform
・ X-ray transient
・ X-ray tube
・ X-ray vision
・ X-Ray Vision (album)
・ X-linked dominant inheritance
X-linked endothelial corneal dystrophy
・ X-linked hypertrichosis
・ X-linked hypophosphatemia
・ X-linked ichthyosis
・ X-linked intellectual disability
・ X-linked lymphoproliferative disease
・ X-linked myotubular myopathy
・ X-linked recessive chondrodysplasia punctata
・ X-linked recessive hypoparathyroidism
・ X-linked recessive inheritance
・ X-linked reticulate pigmentary disorder
・ X-linked severe combined immunodeficiency
・ X-linked spinal muscular atrophy type 2
・ X-Lite
・ X-M1


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X-linked endothelial corneal dystrophy : ウィキペディア英語版
X-linked endothelial corneal dystrophy

X-linked endothelial corneal dystrophy (XECD) is a rare form of corneal dystrophy described first in 2006, based on a 4-generation family of 60 members with 9 affected males and 35 trait carriers, which led to mapping the XECD locus to Xq25. It manifests as severe corneal opacification or clouding, sometimes congenital, in the form of a ground glass, milky corneal tissue, and moon crater-like changes of corneal endothelium. Trait carriers manifest only endothelial alterations resembling moon craters.
As of December 2014, the molecular basis for this disease remained unknown, although 181 genes were known to be within the XECD locus, of which 68 were known to be protein-coding.
==References==


抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
ウィキペディアで「X-linked endothelial corneal dystrophy」の詳細全文を読む



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