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4). The compound, Cs 3 CdH 5, prepared by the reaction of caesium hydride, CsH, and cadmium metal powder at high temperature contains the CdH 2− 4 ion, along with caesium cations, Cs +, and hydride anions, H −. The tetrahedral anion is an example of an ionic complex of CdH 2. The average Cd-H bond length in CdH 2− 4 is 182pm.
View/Edit Mouse. Cadherin-4 is a protein that in humans is encoded by the CDH4 gene. [5] [6] [7] This gene is a classical cadherin from the cadherin superfamily. The encoded protein is a calcium-dependent cell-cell adhesion glycoprotein composed of five extracellular cadherin repeats, a transmembrane region and a highly conserved cytoplasmic tail.
Congenital diaphragmatic hernia ( CDH) is a birth defect of the diaphragm. The most common type of CDH is a Bochdalek hernia; other types include Morgagni hernia, diaphragm eventration and central tendon defects of the diaphragm. Malformation of the diaphragm allows the abdominal organs to push into the chest cavity, hindering proper lung ...
There’s no cure for stage 4 chronic kidney disease. The goal of treatment is to prevent kidney failure and maintain a good quality of life. Your life expectancy will depend on several factors ...
Shortness of breath. Problems with exercise. The symptoms of congenital heart disease in infants and children may include: A bluish tint to the skin, fingernails, and lips (cyanosis, a condition ...
Cadherin-1 or Epithelial cadherin (E-cadherin), (not to be confused with the APC/C activator protein CDH1) is a protein that in humans is encoded by the CDH1 gene. [5] Mutations are correlated with gastric, breast, colorectal, thyroid, and ovarian cancers. CDH1 has also been designated as CD324 ( cluster of differentiation 324).
Congenital heart defect. A congenital heart defect ( CHD ), also known as a congenital heart anomaly, congenital cardiovascular malformation, and congenital heart disease, is a defect in the structure of the heart or great vessels that is present at birth. [7] A congenital heart defect is classed as a cardiovascular disease. [10]
1 in 1,000 (term babies) [3] Hip dysplasia is an abnormality of the hip joint where the socket portion does not fully cover the ball portion, resulting in an increased risk for joint dislocation. [1] Hip dysplasia may occur at birth or develop in early life. [1] Regardless, it does not typically produce symptoms in babies less than a year old. [3]