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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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Introduction and causes of Williams syndrome


Williams syndrome is a rare genetic disorder that causes a variety of symptoms and learning issues. Children with this syndrome could have problems with their hearts, blood vessels, kidneys, and other organs. Their nose, mouth, and other facial features may be unique. They sometimes have trouble learning.

Children with Williams syndrome will need to see many doctors throughout their lives. But with the right treatment, they can stay healthy and do well in school.

CAUSES

Babies with Williams syndrome are born without certain genes. The symptoms they have depend on the genes they're missing. For example, someone born without a gene called ELN will have heart and blood vessel problems.

The genes are usually missing in the sperm or egg before they meet up to form the baby. In a small number of cases, babies inherit the genetic deletion from a parent with the condition, but it is usually a random disorder in the genes.

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