Abandoned Child Syndrome Questions

You need to take Folic acid 5 mg regularly and get Ultrasounf for NT and NB and double marker at 11 weeks to rule out any problem of the baby. If all reports are fine then you can keep the baby.

Klinefelter can be confirmed only by chromosomal study, there are lots of other features you have not mentioned. based on what u say alone it cannot be diagnosed. Good luck

You are worrying unnecessarily. If it's bothering you consult a geneticist and get your chromosome pattern.

Hi lybrate-user. Trying with due respect is your part. To reply it or not or in positive or negative is no her part.
Obviously you should not sacrifice your study.
After few years she may not matter much but your study will matter whole life.
So see the priority and concentrate on that.

Don't worry. You and your wife will be fine. Only thing is that she might have to undergo a cesarean section.

Can not say for sure. She is not deaf. That matters. Go ahead and get married. Genetics is a complex science.

Little higher chances of hereditory diseases among close relatives. No more specific answers can be given unless there is some disease detected in family.

The best time to get a scan that rules out congenital anamoly in foetus is 18 -24 weeks scan .Any scan done after that might have high chance of missing anamolies in the baby. That is what they have mentioned. As long as the growth of the baby in the scan you have done is adequate do not worry about the comment.

Use syp Carnikid 5 ml twice a day. It's new remedy by astrum pharma for muscular dystrophies n delayed developmental problems.

Appetite stimulants, although efficacious in treating malnutrition in CF, should only be prescribed if decreased food intake secondary to inadequate appetite is the principal cause of the malnutrition and all other contributing factors have been assessed, ruled-out or treated. the use of several appetite stimulants used in CF and other diseases to improve appetite and maximize caloric intake