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・ Congenital cataract
・ Congenital chloride diarrhea
・ Congenital clasped thumb
・ Congenital contractural arachnodactyly
・ Congenital contractural arachnodactyly in cattle
・ Congenital cutaneous candidiasis
・ Congenital cytomegalovirus infection
・ Congenital dermal sinus
・ Congenital diaphragmatic hernia
・ Congenital disorder
・ Congenital disorder of glycosylation
・ Congenital disorder of glycosylation type IIc
・ Congenital disorders of amino acid metabolism
・ Congenital distal spinal muscular atrophy
・ Congenital dyserythropoietic anemia
Congenital dyserythropoietic anemia type I
・ Congenital dyserythropoietic anemia type II
・ Congenital dyserythropoietic anemia type III
・ Congenital dyserythropoietic anemia type IV
・ Congenital epulis
・ Congenital erosive and vesicular dermatosis
・ Congenital estrogen deficiency
・ Congenital fiber type disproportion
・ Congenital fibrosis of the extraocular muscles
・ Congenital fourth nerve palsy
・ Congenital generalized lipodystrophy
・ Congenital hearing loss
・ Congenital heart defect
・ Congenital Heart Surgeons' Society
・ Congenital hemolytic anemia


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Congenital dyserythropoietic anemia type I : ウィキペディア英語版
Congenital dyserythropoietic anemia type I
Congenital dyserythropoietic anemia type I (CDA I) is a disorder of blood cell production, particularly of
the production of erythroblasts, which are the precursors of the red blood cells (RBCs).〔http://www.enerca.org/anaemias/24/congenital-dyserythropoietic-anaemia-type-i〕
==Genetics==
CDA type I is transmitted by both parents autosomal recessively and usually results from mutations in the CDAN1 gene. Little is known about the function of this gene, and it is unclear how mutations cause the characteristic features of CDA type I. Some people with this condition do not have identified mutations in the CDAN1 gene, leading researchers to believe that mutations in at least one other gene can also cause this form of the disorder.〔http://ghr.nlm.nih.gov/condition/congenital-dyserythropoietic-anemia〕

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