Newborn infant disorders

Our neonatal care specialists are medically equipped and trained to handle virtually any problem that you or your baby may encounter before, during or following birth. From taking care of mothers with high-risk pregnancies to treating at-risk newborns, our medical team is ready to serve your family. Some of the most common newborn conditions we treat include:

  • Birth asphyxia
  • Birth defects
  • Breathing problems
  • Cardiac failure
  • Congenital heart disease
  • Fetal alcohol syndrome
  • Fetal ethanol exposure
  • Gastrointestinal disorders
  • Hematologic conditions
  • Infections
  • Inherited metabolic disorders
  • Low birth weight
  • Malformation syndromes
  • Neonatal lung injury
  • Neurological problems
  • Premature birth
  • Severe respiratory distress
  • Sleep apnea
Health Encyclopedia

Chromosome

Chromosomes and DNA
Chromosomes and DNA

Definition

  

Chromosomes are long pieces of DNA found in the center (nucleus) of cells. DNA is the material that holds genes. It is considered the building block of the human body.


Information

  

Chromosomes come in pairs. Normally, each cell in the human body has 23 pairs of chromosomes (46 total chromosomes). Half come from the mother; the other half come from the father.

Two of the chromosomes (the X and the Y chromosome) determine if you are born a boy or a girl (your gender). They are called sex chromosomes:

  • Females have 2 X chromosomes.
  • Males have 1 X and 1 Y chromosome.

The mother always contributes an X chromosome to the child. The father may contribute an X or a Y. Therefore, it is the father that determines the gender of the child.

The remaining chromosomes are called autosomal chromosomes. They are known as chromosome pairs 1 through 22.

Related topics:

For detailed information, see heredity and disease (genetics).


 
Review Date: 1/16/2007
Reviewd By: Brian Kirmse, MD, Mount Sinai School of Medicine, Department of Human Genetics, New York, NY. Review provided by VeriMed Healthcare Network.
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