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Cholestatic liver disease is a condition that results from an impairment of bile formation or bile flow to the gallbladder and duodenum (first section of the small intestine). ... The effects of cholestasis are profound and widespread, leading to worsening liver disease and systemic illness.
Primary biliary cholangitis (PBC), formerly known as primary biliary cirrhosis, is a chronic liver disease resulting from progressive destruction of the bile ducts in the liver – called the intrahepatic bile ducts. Bile produced in your liver travels via these ducts to your small intestine where it aids in the digestion of fat and fat-soluble vitamins (A, D, E and K). When the ducts are destroyed, bile builds up in the liver contributing to inflammation and scarring (fibrosis). Eventually this can lead to cirrhosis and its associated complications, as scar tissue replaces healthy liver tissue and liver function becomes increasingly impaired.
What is syndrome of inappropriate antidiuretic hormone (SIADH)? Well, SIADH is a condition where too much ADH hormone is released, which causes an increase in blood volume and ultimately leads to a series of complications related to the blood osmolality and osmolarity
Bartter syndrome has traditionally been classified into three main clinical variants, as follows: Neonatal (or antenatal) Bartter syndrome Classic Bartter syndrome Gitelman syndrome Advances in molecular diagnostics have revealed that Bartter syndrome results from mutations in numerous genes that affect the function of ion channels and transporters that normally mediate transepithelial salt reabsorption in the distal nephron segments. Hundreds of mutations have been identified to date. Such advances may result in the development of new therapies (see the image below). [2] (See Pathophysiology and Etiology.)
Liddle syndrome is an inherited form of high blood pressure (hypertension). This condition is characterized by severe hypertension that begins unusually early in life, often in childhood, although some affected individuals are not diagnosed until adulthood. Some people with Liddle syndrome have no additional signs or symptoms, especially in childhood. Over time, however, untreated hypertension can lead to heart disease or stroke, which may be fatal.
Bartter syndrome, originally described by Bartter and colleagues in 1962, [1] represents a set of closely related, autosomal recessive renal tubular disorders characterized by hypokalemia, hypochloremia, metabolic alkalosis, and hyperreninemia with normal blood pressure. The underlying renal abnormality results in excessive urinary losses of sodium, chloride, and potassium.
Formerly called toxemia, preeclampsia is a condition that pregnant women develop. It is marked by high blood pressure in women who have previously not experienced high blood pressure before. Preeclamptic women will have a high level of protein in their urine and often also have swelling in the feet, legs, and hands. This condition usually appears late in pregnancy, generally after the 20 week mark, although it can occur earlier
Developmental Psychology Documentary on Brain and Intelligence Development in Babies SHOW MORE
Scientists have found that every baby has genius potential, a child's education must begin early in order to develop the potential it has. Pregnancy is not too early to start, as evidence indicating that the developing fetus can learn is ever mounting.
uses video of babies and toddlers to show the communication milestones expected in typically developing children. She also discusses what parents should do if they suspect their child is developmentally delayed
Developmental Milestones: Baby Talk from First Sounds to First Words
the motor milestones expected in typically developing babies, from head control to walking and what pediatricians look for during a well-baby visit. She also explains the specific types of motor control a baby must master before the next milestone can be achieved
New dental fillings could allow your teeth to heal themselves.
You May Be Able to Repair Cavities Without Getting a Filling
The Distal Femoral Osteotomy System utilizes the same principles of design featured in the Tibial Osteotomy System. Specifically designed femoral osteotomy plates take into account the anatomical differences between the distal femur and proximal tibia.
This is a technique of correcting knock knee (genu valgum) deformity by surgery. Highligh of the technique is that the bone is not cut, but merely weakened. The advantage is that it provides accuracy to the surgeon, and rapid healing. Once corrected, the bone is held in place with a special plate (Tomofix), which permits walking with crutches the very next day.
Here is how surgeons perform knock knee correction surgery. Titanium plate is used to stabilize the affected area. The femur is cut nearly through to help with the stability. Spreaders angle the cut align the leg. The plate is secured with several screws. Synthetic bone graft material is packed in the joint. The patient will be in crutches for 4 to 6 weeks.
Helping Babies Born with Drug Addiction. see to learn more
Each year, thousands of babies in the U.S. are born addicted to opiates. And the problem is getting worse.
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