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Symptoms of Rubella in newborns

Contingent upon while during the pregnancy the embryo is contaminated, it might have no indications or might be stillborn. Babies who endure may have various birth deserts. These birth absconds are alluded to as congenital rubella syndrome (CRS).  The most well-known indications of innate rubella disorder in infants incorporate: Low birth weight  Small head/ Microcephaly   Brain inflammation Cataracts Damage to the retina Hearing loss Heart defects Enlarged liver and spleen Bruises or other skin spots Enlarged lymph nodes
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Diagnosis and Treatment of Trisomy 18

DIAGNOSED

A doctor may suspect trisomy 18 during a pregnancy ultrasound, although this isn't an accurate way to diagnose the condition. More precise methods take cells from the amniotic fluid (amniocentesis) or placenta (chorionic villus sampling) and analyze their chromosomes.

After birth, the doctor may suspect trisomy 18 based on the child's face and body. A blood sample can be taken to look for chromosome abnormality. The chromosome blood test can also help determine how likely the mother is to have another baby with trisomy 18.

If you are concerned that your baby may be a risk for trisomy 18 because of a past pregnancy, you may want to see a genetic counselor.

TREATMENT

There is no cure for trisomy 18. Treatment for trisomy 18 consists of supportive medical care to provide the child with the best quality of life possible.
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