MedGEN
  • Home
  • Services
    • Non Invasive Prenatal Testing
      • Introduction to NIFTY
      • Why get a NIFTY test?
      • How do I get a NIFTY test?
      • The Science Behind NIFTY
      • Information about Conditions
    • Prenatal Diagnosis
      • CVS
      • Non Invasive Prenatal Diagnosis
      • Ultrasound
    • Genetic Carrier Screening
    • Disease Specific Tests
    • New Born Screening
    • Cancers Panels
    • Cardiovascular Panels
    • Genetic Counselling
  • Test Information
    • Sample Requirement
    • Packing Requirements
    • Sample Courier (Pick Up)
    • Special Instructions
  • Contact

1275 York Avenue

New York, NY 10065

24x7 Alll Time

No Closed Time
042-35233935

Information about Conditions

Home » Services » NIFTY: Non Invasive Prenatal Testing » Information about Conditions
  • Introduction to NIFTY
  • Why get a NIFTY test?
  • How do I get a NIFTY test?
  • The Science Behind NIFTY
  • Information about Conditions
  • Trisomies
  • Deletion Syndromes
  • Sex Chromosomal Aneuploidy

A trisomy is a term for a genetic condition in which there are three chromosomes instead of the usual pair.

Trisomy 21 / Down Syndrome:

Trisomy 21, more commonly known as Down Syndrome, is a condition caused by an extra copy of chromosome 21. Unfortunately, miscarriage occurs in about 30% of pregnancies with Down Syndrome. Those children born with Down Syndrome will need extra medical care depending on the child’s specific health problems. Most children with Down Syndrome have intellectual disabilities that range from mild to moderate.

Trisomy 18 / Edwards Syndrome:

Trisomy 18, or Edwards Syndrome, is caused when a baby has three copies of chromosome 18, instead of two. Unfortunately, pregnancies with Edwards Syndrome are at high risk of miscarriage and most babies born with Edwards Syndrome die within the first few weeks of life while less than 10% live beyond one year. Infants with Edwards Syndrome have severe intellectual disabilities and birth defects typically involving the heart, brain, and kidneys, and external abnormalities such as cleft lip/palate, small head, club feet, underdeveloped digits, and small jaw.

Trisomy 13 / Patau Syndrome:

Trisomy 13, or Patau Syndrome, is caused when a baby has three copies of chromosome 13, instead of two. Unfortunately, pregnancies diagnosed with Patau Syndrome are at high risk for miscarriage or stillbirth, and most babies born with Patau Syndrome will not survive beyond the first weeks of life. Babies with Patau Syndrome may have heart defects, brain or spinal cord problems, extra fingers and/or toes, cleft lip/cleft palate, and weak muscle tone. Many babies have birth defects of other organs as well.

Trisomy 22

Trisomy 22 is caused when a baby has three copies of chromosome 22, instead of two. Trisomy 22 is very rare. Unfortunately, pregnancies diagnosed with trisomy 22 are at very high risk of miscarriage or stillbirth.

Trisomy 16

Trisomy 16 is caused when a baby has three copies of chromosome 16, instead of two. Full trisomy 16 is incompatible with life and unfortunately most women will miscarry in the first trimester.

Trisomy 9

Trisomy 9 is caused when a baby has three copies of chromosome 9, instead of two. Babies born with trisomy 9 commonly have defects in the heart, kidneys, and musculoskeletal system.

About This Site

MedGEN is the leading company providing a range of genomic screening services in Pakistan. We have a vast experience of working with and prevention of different genetic conditions in the country. The genomic services provided by MedGEN include Non-Invasive Prenatal Test, Invasive Prenatal Diagnosis, Carrier Screening, Genetic Diagnosis, New Born Screening and Genetic Counselling.

Find Us

Address
167 B, PCSIR II, Lahore, Pakistan

Contact
0304-4124272
042-35233935

Email
medgenpakistan@hotmail.com

Announcements

  • 2nd World Congress on HUMAN GENETICS
    Genomic Revolution: A debate on Human Genetic Disorders & Diseases. September 14-15, 2017 Edinburgh, Scotland
  • Thalassaemia International Federation
    14th International Conference on Thalassaemia & Haemoglobinopathies & 16th TIF International Conference for Patients & Parents. 17-19 November 2017 Grand Hotel Palace, Thessaloniki, Greece.
  • 12 National Thalassaemia National Conference & Workshops
    Nov 2017, Quetta, Pakistan. For more information www.tfp.org.pk Tel: 042-35233935
Responsive WordPress Carousel Plugin

Latest News

International Fetal Medicine Long Course

International Fetal Medicine Long Course

April 8, 2017

A six days International Fetal medicine Long Course was organized at the ...

read more

2nd International Conference on Maternal Fetal Medicine

2nd International Conference on Maternal Fetal Medicine

April 11, 2017

The 2nd International Conference on Maternal Fetal Medicine was ...

read more

International Fetal Medicine Workshop

International Fetal Medicine Workshop

April 17, 2017

Thalassaemia Federation of Pakistan organized an International Workshop ...

read more

Copyright © 2015 | Powered by #Tribe
  • Yelp
  • Facebook
  • Twitter
  • Instagram
  • Email