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Severe hereditary heart imperfection commonly becomes obvious soon after the birth of a child or at some point in the first few months of its life. It is a tragic condition in children and some of the symptoms that are associated with the heart imperfections include rapid breathing, grunting while breathing, swelling of the abdomen, legs and areas around the eyes of the baby.
The baby experiences shortness of breath during feeding and in this way, the baby does not gain much weight. The nostrils of the baby also become flared, and they at times turn pale blue in their skin color. In some cases, the blood pressure of the baby is also very low after their birth.
Congenital heart defects are at times not diagnosed in the early stages of childhood as the signs are not noticeable.
However, some of the signs that are obvious and noticeable in older children mainly include:
- Children become short of breath while exercising or doing some activity and at times these children require frequent monitoring.
- They get tired in no time and have less stamina
- The legs of these children suffering from congenital heart defects tend to swell.
- The blood circulation in these children is very poor
- Holes in the heart occur and typically in the walls between the major blood vessels as well as the chambers.
Do Tests Regularly:
It is very important that a follow up is done with pediatrician regularly and the tests described are performed regularly. In any such case if the problem is significant, then it is likely that your medical doctor would refer your child to a paediatric cardiologist. The paediatric cardiologist is specially trained to identify as well as treat severe heart problems in young children, infants and even in young adults.
Medications Used for Treating Heart Disease:
The condition cannot be prevented and hence to lower the risk of your baby having congenital heart disease it is very necessary that women have a healthy pregnancy. There are certain medications provided by the doctors to treat this condition and relieve the symptoms caused. The medications that are used include Vasodilators to widen the blood vessels so that the blood circulation is improved, Diuretics are used to reduce the extra fluid in the body. The strength of the heart beat is increased by use of Digoxin, and irregular heartbeats can be prevented by use of Antiarrhythmics. However, these medications do not treat the defect completely.
Hi doctor I have my daughter age of 1 year hold baby she was got eye surgery in 6 months back for issue with eye cataract buildup. Now doctors said now baby 100% ok with vision. So now baby what ware tha glass for future vision So my questions is how 1 year baby how to maintain tha eye glass for ware please give me suggestions.
An infant is usually called a bundle of joy and with good reason. There are simple and carefree, and bring a smile to your face with their antics. However, the mood and health of an infant can be tarnished due to an issue which is known as galactosemia.
What is Galactosemia?
When a baby has galactosemia, he or she will have a problem when it comes to digesting galactose, which is something that is present not only in milk but in all milk products. Galactose is a sort of sugar, just like fructose and glucose is. As a matter of fact, lactose, which is what milk has, is, in fact, a combination of glucose and galactose. Also, when lactose is processed, it is broken down by the human body into its constituents.
The condition is something that is passed down through the genes of the parents of the baby. The condition would occur if the gene which causes a tendency for a baby to have galactosemia is present not only in one parent but both of them. A baby who has the condition will be lacking an enzyme which is known as the GALT enzyme. The enzyme could also not be functioning as it should be under normal circumstances.
When it comes to the problem, it is very important, to say the least, to detect it sooner rather than later as if there is a build-up of unprocessed galactose which is allowed to occur, it can affect the baby adversely and in some cases, it can also be threatening to the life of the baby!
How does it affect a baby?
The problems which can erupt due to galactosemia include issues which affect organs such as the brain, eyes, liver and kidneys. It is interesting to take note of the fact that these are all organs which either have something to do either processing the blood or are heavily dependent on it. While a baby is not in the position in which he or she can communicate the issues that are being faced, when keeping an eye out for galactosemia, the signs which are displayed include an irritability of the baby as well as lacking consumption of the milk of the mother.
Even though galactosemia may not be the case, a doctor should be consulted as the exacerbated issue can include seizures and jaundice. It is to be kept in mind that galactose is something that can be found not only in the milk of the cow but also human milk as well as the milk of other animals such as goats.