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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

Congenital Heart Defects (CHDs)

A congenital heart defect is a flow defect in blood flow through a heart.  This may cause block or slow down in a blood flowing heart. This causes the abnormal flow of blood through the heart and making the heart work harder. It is an abnormal formation of the heart during growth in the womb. Abnormality in the number of baby chromosomes through the source of single gene defects from parents and also from environmental sources.

 

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TYPES 

    This may vary from simple to complex forms of CHDs. They are,

  • Ventricular septal defects
  • Tetralogy of Fallot
  • Transposition of great arteries 
  • Atrioventricular septal defects
  • Coarctation of aorta 

Some of the flow defects such as Atrial & Ventricular septal defects.Blood flow from the left side to the right side such as left to right shunts.

GROUP

  1. Cyanotic - Bluish discoloration of lips, gums, and skin ( circulation of blood does not have enough oxygen )
  2. Acyanotic - not have the condition of cyanosis.

MATERNAL FACTORS 

When a mother comes in contact with some type of substance in 1st few weeks of pregnancy. This is a time the baby's heart is in growth. Some illness of the mother may have or medicine for illness causes heart growth.

OTHER HIGHER RISK FACTORS       

  • Seizure
  • PKU
  • Depression
  • Insulin-dependent diabetes
  • Invitro fertilization
  • Rubella ( MMR vaccine)
  • Lupus
  • Connective tissue disorder   

 FAMILY HISTORY & CHDs           

It is an Autosomal dominant inheritance. About  1% of all children. First-degree relatives are at a higher risk of CHDs. 

First-degree relatives 

CHROMOSOMAL ABNORMALITIES    

In each cell body of a living being has 46 chromosomes. Having too many or too few chromosomes causes CHDs.  They may also cause structural defects that are missing half several chromosomes.  

                                  

Comments

  1. can you post about,how to identify the heart issues when the baby before birth.

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