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Indications for cytogenetic testing

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Pregnancy losses, bad obstetric history, infertility, young adults with developmental problems, children with delayed milestones, dysmorphology, mental retardation are tested for chromosomal anueploidy or subtle structural defects. Reports include detailed interpretation and a high resolution karyotype format picture generated through automated image analysis systems.

Indications Test recommended Code
Bad obstetric history
Primary Infertility
Amenorrhea
Azoospermia, Oligospermia and other sperm defects
Couples planning for ICSI or IVF
Children with developmental problems, delayed milestones
Children with dysmorphology, congenital defects
Mental retardation
Neonates with ambiguous genitalia
Blood Karyotyping or Chromosomal analysis or Cytogenetic testing CYT01
Prader-Willi syndrome
Angelman syndrome
Smith-Magenis syndrome
Miller-Dieker syndrome
Other micro-deletion syndromes
High resolution banding karyotyping CYT02
First trimester pregnancy loss
Second or third trimester pregnancy loss
Aborted products for abnormal ultrasound findings and multiple fetal defects like Cystic hygroma, Fetal hydrops, Duedinal atricia, Hydrocephaly, Omphalocele, Fetal cardiac defects
Intra Uterine Death (IUD)
Intra Uterine Growth Retardation (IUGR)
Products of Conception Karyotyping CYT03
Fetal Cord blood, Fetal Heart blood Karyotyping (Post-delivery or abortion) CYT04
Risk positive results after prenatal screening (first trimester or triple screen test)
Conception after prolonged infertility or artificial reproductive methods
Previous history of genetic defects in the family
Bad obstetric history
Abnormal ultrasound findings and fetal defects like like Cystic hygroma, Fetal hydrops, Duedinal atricia, Hydrocephaly, Omphalocele, Fetal cardiac defects, Oligohydramnios, Polyhydramnios, IUGR
Prenatal Cord blood Karyotyping CYT05
Prenatal Amniotic fluid Karyotyping CYT06
Prenatal Chorionic villus sample (CVS) Karyotyping CYT07

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