نتایج جستجو برای: disease progression
تعداد نتایج: 1600776 فیلتر نتایج به سال:
Morquio's syndrome is an autosomal recessive disease. It is from mucopolysacaridosis group disease and it's obvious clinical signs are severe skeletal dysplasia and normal intelligence. Deposition of keratan sulfate in different tissues is seen and with progression of the disease, connective tissue of cornea, airways, lung and heart valves will be involved. In this article we present a case of ...
dysplasia epipysealis hemimelica (deh) is a rare disease, prevalence is one in 1000000. the incidence is unknown. its characteristics is abnormal cartilage growth accompanied by ossification of cartilages of epiphyses of long bones, bones of foot ankle and wrist. a hereditary or familial factor hasn't yet been known. occurrence in males is three times more than females. our case is a girl ...
A single nucleotide polymorphism (SNP) in CD24 has been associated with multiple sclerosis (MS) in a population based study. This SNP results in the replacement of alanine (CD24A) by valine (CD24V) at amino acid 57 in the resulting polypeptide chain. In the current study, the genotyping of this SNP and its contribution to MS in 217 patients and 200 healthy individuals of an Iranian population w...
نمودار تعداد نتایج جستجو در هر سال
با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید