What are the signs & symptoms of Pediatric Craniosynostosis
Following are the common signs and symptoms of pediatric craniosynostosis. An abnormal feeling or disappearing fontanel (soft spot on the top of the head) Asymmetrical, misshapen skull Development of a raised, hard ridge along with the skull Slow or no growth of the head as the baby grows
These conditions can be corrected with surgery and can restore.
What are the different types of Pediatric Craniosynostosis?
Craniosynostosis can affect babies in two different ways Isolated craniosynostosis: Isolated craniosynostosis known as non-syndromic craniosynostosis, is the closing of only one suture with no other associated health problems and is the most common kind of craniosynostosis. Syndromic craniosynostosis: Syndromes are when three or more medical problems occur in a recognizable pattern. When craniosynostosis is part of a syndrome, it is known as syndromic craniosynostosis. In these cases, there are usually two or more sutures that closed too early. Patients also have other health conditions as part of the syndrome.
What is Pediatric Craniosynostosis?
The skull is formed by several separate bones. These skull bones are connected by specialized structures called sutures. These sutures look like seams or spaces between the skull bones. The sutures are growth centers for the skull bones. Craniosynostosis is present when one or more of the sutures closes earlier than it should cause the skull to grow into an abnormal shape.
Babies' brains grow very quickly in the first two years of life. As the brain grows it stretches the sutures which signal the sutures to make new bone. The sutures allow the skull to enlarge and create just enough space for the brain. Normally, these sutures remain open until we reach adulthood, long after the brain and skull have stopped growing. Craniosynostosis causes a baby’s skull to misshapen because the brain continues to grow at the same rate even if one or more sutures close too early.
The remaining open sutures have to grow faster to make up for the closed suture. This extra growth causes a change in head shape. In some cases, the remaining open sutures can’t grow fast enough to keep up with the brain’s growth causing abnormally high pressure in the skull, which can have negative effects on brain health. These include learning delays, blindness, and, rarely, death, if untreated.
What is scoliosis spine surgery?
Scoliosis spine surgery is a specialised surgery for correction of spine deformity
Are spinal deformity surgeries safe?
Yes, these surgeries are safe. The centre for spine care at Aster Medcity has the latest medical technology for ensuring maximum patient safety and are performed with the help of intra-operative nerve monitoring for unmatched accuracy.
Why test sudomotor function?
A sudomotor function test is a quick and reliable way of identifying certain types of neuropathies. The presently available tests detect only 50-60% of neuropathies. This test helps the clinician to identify small fiber neuropathies and improve diagnostic accuracy.
Are there any side effects of undergoing bariatric surgery?
The side effects of bariatric surgery are relatively lesser compared to the health issues that you suffer from obesity. Some side effects may include general weakness, malnutrition, temporally hair loss. You can overcome these issues by following the guidelines from dietitian and doctor.
What are the types of liver cancer (Hepatocellular carcinoma)?
There are mainly five types of liver cancer based upon the type of cell in the liver. Hepatocellular carcinoma (HCC) Hepatocellular carcinoma (HCC) is a common type of primary liver cancer which affects the main liver cells called hepatocytes. People with cirrhosis and men are more prone to get Hepatocellular Carcinoma. Fibrolamellar carcinoma Fibrolamellar carcinoma is rare liver cancer, it comes as a subtype of Hepatocellular carcinoma and usually seen in healthy teens and adults under 40 years old. Interestingly, people diagnosed as Fibrolamellar carcinoma is not usually associated with liver cirrhosis or Hepatitis B or C infection. Cholangiocarcinoma (bile duct cancer) Cholangiocarcinoma is a rare liver cancer of the bile ducts, also categorized under primary liver cancer. The carcinoma begins in the section of ducts inside the liver is called intrahepatic cholangiocarcinoma. Angiosarcoma Angiosarcoma a type of rare liver cancer affects the blood vessels of the liver; it is commonly seen in the elderly population. Angiosarcoma is also known as soft tissue sarcoma or haemangiosarcoma. Hepatoblastoma: Hepatoblastoma is a kind of rare primary liver cancer that mainly affects children under 3 years old.
How liver cancer is diagnosed?
Liver cancer is diagnosed by performing following tests and procedures; It is not possible to diagnose hepatic cancer by doing normal blood tests. A specific blood test is done to find levels of alfa-fetoprotein in serum (AFP). Increased levels of AFP indicate presence of liver cancer. Sometimes the doctor may suggest imaging studies such as a CT or MRI scan. Liver biopsy is another method used to identify malignant or benign tumour. It is done is by removing tissue from liver and examining under the microscope, liver biopsy can be done along with CT scan. Another method to identify liver cancer is by doing laparoscopy, in this procedure the surgeon assesses the signs of hepatocellular carcinoma by inserting a flexible tube with a camera and light at the tip (laparoscope) by making a small incision in the abdomen.
How do alcohol-related liver diseases progress?
Heavy drinkers usually progress from fatty liver to alcoholic hepatitis to alcoholic cirrhosis over time. However, one may develop alcoholic cirrhosis without getting alcoholic hepatitis first. Besides, obesity, diabetes and chronic Hepatitis C infection increase the chance of liver diseases substantially.

