Search results
Results from the WOW.Com Content Network
Kidney function may be normal in the first weeks or months of life. [3] Laboratory studies show low serum levels of protein (albumin) and immunoglobulins, and elevated levels of triglycerides and cholesterol. [1] Blood work may also show thyroid and vitamin D deficiency. [1] Kidneys on ultrasound imaging may appear enlarged and brighter ...
Multicystic dysplastic kidney (MCDK) is a condition that results from the malformation of the kidney during fetal development. The kidney consists of irregular cysts of varying sizes. Multicystic dysplastic kidney is a common type of renal cystic disease, and it is a cause of an abdominal mass in infants. [5]
Perlman syndrome (PS), also known as nephroblastomatosis-fetal ascites-macrosomia-Wilms tumor syndrome, is a rare overgrowth syndrome caused by autosomal recessive mutations in the DIS3L2 gene.
Baby Alex only lived for two days, but he helped researchers better understand the rare kidney disease that caused his death. Daria recently had a baptism, and the Volkovs are settling into ...
Nephromegaly is the process whereby a kidney or both kidneys become enlarged. [1] Both autosomal dominant and autosomal recessive polycystic kidney disease can cause nephromegaly. [ citation needed ]
For premium support please call: 800-290-4726 more ways to reach us
Autosomal recessive polycystic kidney disease (ARPKD) is the recessive form of polycystic kidney disease. It is associated with a group of congenital fibrocystic syndromes. [ 5 ] Mutations in the PKHD1 (chromosomal locus 6p12.2) cause ARPKD.
Renal agenesis is a medical condition in which one (unilateral) or both (bilateral) fetal kidneys fail to develop. Unilateral and bilateral renal agenesis in humans, mice and zebra fish has been linked to mutations in the gene GREB1L. [1] It has also been associated with mutations in the genes RET or UPK3A [2] in humans [3] and mice respectively.