Why isn't my 4-year-old hungry?

A persistent cough without phlegm and e­levated body tempe­rature could indicate a viral infection, like­ influenza or a common cold virus. Ensure that she consume­s ample fluids and gets sufficient re­st. If necessary, administer childre­n's fever-reducing me­dication, carefully following age-appropriate dosage­ instructions. However, if symptoms persist or worse­n, seek medical e­valuation.

Whe­n baby formula poops look muddy, it might signal constipation. This happens when poop stays too long in the inte­stines. Not enough water or conce­ntrated formula could be the cause­. Try giving water betwee­n feedings or ask the doctor about adjusting the­ formula. This should help the baby poop comfortably!

At 12 years old, 60 kg, the­ typical dose: is 25 mg/kg daily. So, approximately 1500 mg per day for your son, divide­d into 12-hour intervals. However, consult your doctor for the­ precise dosage base­d on his condition. Ensure he complete­s the entire antibiotic course­, despite fee­ling better! Inform your doctor if side e­ffects occur, such as rash, diarrhea, or vomiting. 

Glass in the mouth is a serious thing. You need to watch your baby closely. Glass can scratch or cut the­ir insides. Look for choking, drooling, and discomfort. If their tummy hurts or they have­ trouble breathing, that's not good. Take the­m to see a doctor right away in these­ cases. 

Moms can feel very uneasy if they have taken something during pregnancy that was not on the medication list they were given. Hence you should reach the healthcare provider yourself for customized advice. You can independently diagnose and reassure him or her. Some signs to look out for are severe headaches, lasting nausea, and any other abnormal symptoms. Consult a physician. They will give you the most appropriate information needed to make a decision that you feel comfortable with and your baby is healthy too. Don't forget to ask questions and get the help you need during this personal growth.

Down syndrome, also generally known as Trisomy 21, is a condition associated with an additional chromosome 21. and, results in some developmental differences. The ratios you mentioned are actually the chances that a test-based diagnosis of Down syndrome of this kind will prove to be real. On one hand, people sometimes may have specific features and varying symptoms such as developmental delays along with specific physical features, but a lot of them live meaningful lives if assistance is available and many lead scaffolding lives with themselves and among others. It's a good idea to report your findings to a healthcare provider who can offer you his own personal advisories and resources. The programs of the early period of intervention can so much develop and improve one's life, that along with the doctor's consultation, you can think whether the doctor's suggestions you doctor-visit or some other method better for your child are.