Doctor insights on:
Smelling Disorders In Children
Smelling disorders: Smelling disorders = conditions affecting olfaction.Get a more detailed answer ›
They aren't: This is a condition where the signals for neuronal development were not followed correctly and resulted in abnormal brain formation. This results in profound developmental impairment and intellectual difficulties. Treatment is supportive. ...Read more
Yes, beginning with: Family history of Specific Language Impairment &/or Dyslexia. Early Expressive Developmental Language Disorder with or without Receptive DLD increases risk even if language "catches up" by 4. Persistent Expressive DLD past 4, diagnosed as SLI, carries a 40-75% risk of Dyslexia. Deficits in sound-symbol association, like P-puh, in pre-school & in phonological awareness in KG are highly predictive. ...Read more
Patience: It's easy to be frustrated with a child who is angry, sullen, amotivated, has a drop in grades, is defiant, looks sloppy etc. Those are behaviors that might be seen in a depressed child. A bipolar child may be even more of a handful. When I work with difficult people, I just keep reminding myself that they are suffering. This allows me to feel some empathy - especially when I am losing patience. ...Read more
Be supportive: Children with mood disorders have a lot of emotions, anxiety, sadness/depression, irritability and sometimes feel that no one cares about them. Encouraging them to do their best and showing them you care and believe in them helps them to feel safer around you and may help them to be more receptive to your instructions. Most children like to please adults and will do their best if they trust you. ...Read more
3 to 5%: Did you mean scheuermann disease? For this diagnosis, genetic factors are more important than environmental ones, but we haven't been able to find specific genes that cause it. Most likely, it's a combo of genes and environmental influences. In conditions with this sort of multifactoral inheritance, the risk for each child of an affected parent is about 3 to 5 percent, or 1 in 20 to 1 in 30. ...Read more
Various diseases: There are many, relatively rare, diseases associated with mitochondrial dysfunction. In children, they can often cause disease states in multiple organs, lead to decreased growth and development and exhibit a wide variety of symptoms. If you have a specific question about a specific type of mitochondrial dysfunction, please feel free to ask! (your doctor). ...Read more
My partner has Crohn's disease and I was wonder what could be the chance of it passing to our children?
Yes: Crohn's disease has many genetic components so it is too complicated to say for sure what the risk is that your children will get crohns. However the risk is definitely elevated above the general population--perhaps a 5-10 fold risk above someone else of your same ethnic background. No screen is necessary but if a child has chronic GI complaints, get them checked out. ...Read more
I was diagnosed with nephritis over 10 years ago, can I have children & will my child inherit this disease from me?
I was diagnosed with nephritis over 10 yrs ago. Is this hereditary? Will my children inherit this disease from me?
Depends on type: Nephritis means "inflammation of the kidney" and has many different causes including post streptococcal nephritis, lupes nephritis, membranoproliferative nephritis etc. None of the above are directly inherited. However there is a disease called "alports syndrome" that is inherited directly. You need to talk to your physician, find out what type of nephritis you had and have him/her advise you. ...Read more
Hello. I was wondering how likely it is for a male Schmidt's syndrome patient to pass on the disease to his children. Thank you.
Risk is there: The genetic risk is there but it doesn't mean all of them will get it. It just means they have a higher chance than the general population to develop the disease. The best thing is to go see the endocrinologist or the geneticist to determine their individual risks. There are test that can be done to determine if they have the antibody and the HLA type ...Read more
Uncle has a type of hemophilia 1 as I do. I want to know what the probablity of my children obtaining this disease and how come?
You have possibly carrier gene. Double recessive gene will express that is disease hemophelia. It was common in the royal family due to in breeding
read up on tramission of genes and inheritable diseases. There is lot of informaltion available reserch on it and will discuss if any more questions. ...Read more
Progeria: Little is known about it.Get a more detailed answer ›
Not necessarily: Lyme is a complex illness. Some who have it become quite ill, while others have mild symptoms. This depends on the strain of lyme bacteria, genetics of the patient, presence of co-infections like babesia & bartonella & factors that affect immune function like nutrition, parasites, heavy metals, mold exposure & stress.Thus, like adults, some children become quite ill but others have minimal symptoms. ...Read more
Immune disorders: Children may be born with immune disorders that affects white blood cell line or immunoglobulins. Based on the kind of deficit the child is not able to fight bacterial / viral/ parasitic infections. Some children have severe combined immunodefiency that affects all cell types. HIV is acquired immunodeficiency. ...Read more
Increased Risk: Incidence of celiac sprue in this country is around 1/130. The niddk has a website for more info, first degree relatives of celiac patients are at much higher risk for developing it. Http://digestive. Niddk. Nih. Gov/ddiseases/pubs/celiac/. ...Read more