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Doctor insights on: Hirschsprung S Disease In Babies

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How rare is huntington's disease in grandkids?

How rare is huntington's disease in grandkids?

Huntington: The classic symptoms start after 30 depending on the number of repeats-the higher the repeats earlier age onset--but juvenile huntington start as teenager when repeats are above 55--an asymptomatic child does not mean he does not have the genetic disorder which will manifest latter--- another group of disorders huntington like start earler does not have the same genetic defect. ...Read more

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Why is fourth baby born with addison disease and other children healthy, ?

Why is fourth baby born with addison disease and other children healthy, ?

Genetic differences: Every child is different- so one may have blue eyes, the another brown, some tall, some short etc. A baby with addison's has a genetic cause- it got genes that the others didn't or had a mutation early in its development. There are many forms of addison's; some are relatively easy to treat, so i hope your baby's form is one of less serious forms. President kennedy & other notables had addison's. ...Read more

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Why is baby born with addison disease?

Why is baby born with addison disease?

Genetic causes: Sorry to hear your baby has addison's. There are several different forms, some more serious than others, & the cause depends on what type of addison's, but generally it is caused by genetic problems from one or both parents or a genetic mutation that occurred early in development. Though the language is rather technical, see http://emedicine.Medscape.Com/article/919077-overview#aw2aab6b2b3aa. ...Read more

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Is hirschsprung's disease a common birth defect?

Is hirschsprung's disease a common  birth defect?

Not so rare: It occurs in about 1 out of every 5,000 newborns and is most common in male babies. Some instances are familial. Down syndrome has fifteen fold increase in incidence of Hirschsprung's disease. ...Read more

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With infantile tay-sachs disease, does the baby always end up handicapped?

With infantile tay-sachs disease, does the baby always end up handicapped?

TaySachs Disease: Yes thevchild ends up handicapped and eventually dies. ...Read more

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How common is celiac disease in children?

How common is celiac disease in children?

Maybe 1% (1 in 100): Celiac disease affects about 1 in 100 people, to about 1 in 150 people. The exact numbers are not certain, but it affects a little less than 1% of the population. ...Read more

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Is hirschsprung disease dangerous to an infant?

Is hirschsprung disease dangerous to an infant?

Can be: Hirschsprung disease has occasionally gone un-diagnosed for a period of time & some kids have developed a severe enterocolitis & died during the illness. With diagnosis, monitoring& treatment a kid can have a realatively normal life. ...Read more

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Is pku and huntington disease the same disease entity?

Is pku and huntington disease the same disease entity?

Some comments: Pku is a problem with children and this needs early diagnosis to prevent profound complications. Huntington's chorea is an autosomal dominant disorder occurring later in life, and is relatively rare, but genetic counseling might be valuable. Neither disorder has any relationship to the other. ...Read more

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Is hirschsprung's disease inheritiable?

Constipation: Hirschsprung's disease is a congenital disease. You are born with it. It causes constipation and /or obstruction due to non functioning of intestinal nerves. It is treatable, but may require surgery to diagnose and treat. In some cases it is heriditary but usually it is sporadic. ...Read more

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What is the disease wegeners granulamatosis in kids?

What is the disease wegeners granulamatosis in kids?

WG: Wegener’s granulomatosis (WG) is a rare disease that causes the walls of blood vessels to become inflamed (called vasculitis). This limits blood flow to tissues and can affect any organ. WG is a type of autoimmune disease. This means the body’s immune system attacks its own tissues. Its cause is unknown. ...Read more

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Frequency of huntington's disease in their children?

Frequency of huntington's disease in their children?

Autosomal dominant : transmission means that each child of a parent with documented Huntington's Disease has a 50% chance of inheriting the mutant gene on Chromosome 4p16. Guidelines for predictive testing are on http://www.hdfoundation.org/html/hdsatest.php. ...Read more

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Can huntington disease be detected before the child is born?

Can huntington disease be detected before the child is born?

With PGD: I suspect that if a pregnancy is conceived by ivf, preimplantation genetic diagnosis could be used to detect which embryos carry the genetic factors to cause huntington's disease, allowing one to only implant embryos that lack that factor. At this point, it cannot be detected in a natural pregnancy, though technology for noninvasive detection of various disorders is under development. ...Read more

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Is crohn disease contagious, how common is it in babies?

Is crohn disease contagious, how common is it in babies?

Crohn's disease: This is not a communicable condition, as far we understand it. Its etiology has been attributed to colonization of the gut with different organisms (a british doctor thinks a tb-like bacillus) and an abnormal host immune response to these. 20% of cases occur in children, but the youngest are in the range of 7-8 years, and often in families with adult crohns, suggesting hereditary component. ...Read more

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How does a baby with congenital heart disease affect the family its born in too ?

How does a baby with congenital heart disease affect the family its born in too ?

Depends: Some problems are relatively simple to fix and after repair will be just fine and require little additional concern. More severe conditions may require multiple surgical procedures and require the allocation of major financial and emotional resources with expected increased stress levels. And some children will never be ok or will die. Good luck. ...Read more

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Would huntington disease be detected before the child is born?

Yes in Mom and child: A gene test can be done on any individual. If the mother carries the gene, she will eventually become symptomatic with huntington disease. Any child of hers will have a 50% chance of inheriting the gene and the disease. Prenatal testing of the child in utero can be performed. Any sort of prenatal testing should involve a genetic counselor consultation, as there are many issues to consider. ...Read more