Background: There are some risk factors being more vulnerable to Lemierre's syndrome such as a hypercoagulable state.
Methods: We report a rare case of Lemier
Background: There are few studies on the genotypes and phenotypes of autosomal recessive polycystic kidney disease in Chinese patients. Methods: PKHD1 mutation
Background: The hypoparathyroidism, deafness and renal dysplasia (HDR) syndrome is an autosomal dominant disorder primarily caused by GATA3 gene mutation. We re