cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test Cost
33,800.00 26,000.00 Book Test
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cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test Cost

33,800.00 26,000.00

-23%

Microdeletion syndromes are caused by the deletion of small portion of genetic material during chromosome duplication. In general, the loss of the genetic material carry risks to childs health and development, such as congenital heart defect, delay development of cognitive impairment, autoimmune disease, etc. Yourgene offer NIPT+ – Microdeletion screen test that includes screening for up to 20 Microdeletion

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Description

cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test Details:

DiGeorge Syndrome (DGS) is the most common microdeletion syndrome which occur one in 2000 births to one in 4000 births. DGS is caused by the loss of small segment of the genes on the long arm of chromosome22. The missing segments cover for 30 to 40 genes and cause the gene expression incomplete. Most people with DGS have underdeveloped organs due to incomplete gene expression, like heart defect, delayed growth, poor muscle tone, difficulty feeding and gastrointestinal problems

List of Yourgene NIPT+ – Microdeletion

List of MicrodeletionRarityCommon Symptoms
Syndrome
DiGeorge syndrome1/2000 to–          congenital heart defect
Jan-00–          cognitive impairments; below borderline normal IQ
 –          autoimmune disorder, etc.
1p36 deletion syndrome1/5000 to–          development delay in growth and learning
1/10000ability
 –          feeding difficulties, etc.
Williams syndrome1/7500 to–          delay development of motor skills
1/20000–          heart murmur, etc.
Koolen-de Vries syndrome1/16000–          feeding difficulties
–          heart defect
–          kidney or urological anomalies, etc.
Prader-Willi syndrome1/15000–          poor muscle tone
–          lack of eye coordination, etc.
Angelman syndrome1/12000 to–          delayed development
1/20000–          intellectual disability
 –          speech impairment
 –          problems with movement and balance (ataxia) , etc.
Smith-Magenis syndrome1/15000 to–          mild to moderate intellectual disability
1/25000–          delayed speech and language skills
 –          distinctive facial features, etc.
Cri-du-Chat syndrome1/20000 to–          severe cognitive, speech, and motor delays
1/50000–          small head size (microcephaly) , etc.
18q deletion syndrome1/40000–          mild to severe intellectual disability
–          mild to severe delayed development, etc.
Wolf-Hirschhorn syndrome1/50000–          distinctive facial features
–          delayed growth and development , etc.
Alagille syndrome1/70000 to–          affect the development of heart, liver, kidney,
1/100000and other system in the body
 –          poor weight gain and growth, etc.
Jacobsen syndrome1/100000–          delayed development
–          bleeding disorder
–          heart defects and congenital heart disease
–          kidney defects, etc.
Hereditary Neuropathy with2-5/100000–          affects peripheral nerves
Liability to Pressure Palsy (HNPP)–          loss of muscle function , etc.
Rubinstein-Taybi syndrome1/100000 to–          short stature
1/125000–          moderate to severe intellectual disability
 –          eye abnormalities, heart and kidney defects, dental problems, obesity , etc.
WAGR syndrome1/500000 to–          aniridia, an absence of the colored part of the
1/1000000eye
 –          reduction in the sharpness of vision (visual acuity) and increased sensitivity to light (photophobia)
 –          intellectual disability , etc.
Potocki-Shaffer syndromeLess than–          affects development of the bones, brain, and
100 case in the worldother organs
 –          intellectual disability, delayed development of speech, motor skills (such as sitting and walking), and social skills , etc.
Miller-Dieker syndromeLess than–          abnormal brain development (lissencephaly)
1/100000–          severe intellectual disability
 –          developmental delay
 –          weak muscle tone , etc.
1q21.1 deletion syndromeLess than–                       developmental delays
100 case in the world–                       mild-to-moderate intellectual disability
 –                       microcephaly, etc.
Kleefstra syndromeLess than–                       severely limited or absent speech
200 case in the world–                       weak muscle tone
 –                       heart defects
 –                       respiratory infections , etc.
Phelan-Mcdermid syndromeLess than–                       moderate to profound intellectual disability
1000 case in the world–                       absent or delayed speech
 –                       autism or autistic-like behavior, etc.

What is cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test ?

cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test is a medical specialty that determines the cause and nature of diseases by examining and testing body tissues (10 ML in Streck tube). It is a cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test that screens for serious conditions.

What type of sample are needed to do a cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test?

A 10 ML in Streck tube for testing can be obtained from several bodily sources. The cells are the most commonly tested are derived.

Standard Biological cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test Samples: 10 ML in Streck tube

How accurate is cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test?

cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test is generally considered to be the most accurate testing method available. DNA Labs India’s cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test  is considered as a benchmark by most doctors. The most precise and accurate cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test in India.

How many days does it take to obtain cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test results?

Results of cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test test are usually available from the laboratory within 1 week to 5 weeks.

For a standard cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test, DNA Labs India returns cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test results in 7 to 10 business days once all samples are received at lab.

DNA Labs India understands that waiting for cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test results for this potentially life-changing test is stressful, so we provide speedy service without sacrificing accuracy.

Once complete, results are posted immediately to our secure online portal, and you will be notified by email right away.

Can cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test be done during pregnancy?

Prenatal cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test is a sensitive subject because of the ethical and legal issues involved, including the risks of an invasive test. You need to talk with your doctor.

How much does a cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test cost?

A standard cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test cost you 26000/- INR.

Why Choose DNA Labs India for cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test?

DNA labs India’s cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test follows with dual testing for 100% accuracy when determining a cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test.

  • We are the leading lab for cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test in India
  • Greater Accuracy
  • Collection centres across India
  • Outstanding customer service
  • Strict privacy and confidentiality assured
  • Full-service laboratories providing testing for use in complex cases

How to Schedule an Appointment for cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test?

You can either book online at the link provided. If you book and make the payment online free home collection service is provided to patients of all cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test.

How can I locate a cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test facility?

DNA labs India has 3000 plus sample collection centres across India for cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test.

You can choose the centre and book the cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test online. For all online bookings made and payment paid a free home sample collection service is provided.

List of cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test collection centres in India are Mumbai, Delhi, Bangalore, Hyderabad, Ahmedabad, Chennai, Kolkata, Surat, Pune, Jaipur, Visakhapatnam, Kanpur, Nagpur, Lucknow, Thane, Bhopal, Indore, Pimpri-Chinchwad, Patna, Vadodara, Ghaziabad, Ludhiana, Agra, Nashik, Faridabad, Meerut, Rajkot, Kalyan-Dombivli, Vasai-Virar, Varanasi, Srinagar, Aurangabad, Dhanbad, Amritsar, Navi, Mumbai, Allahabad, Howrah, Ranchi, Gwalior, Jabalpur, Coimbatore, Vijayawada, Jodhpur, Madurai, Raipur, Chandigarh, Guntur, Guwahati, Solapur, Hubli–Dharwad, Mysore, Tiruchirappalli, Bareilly, Moradabad, Tiruppur, Gurgaon, Aligarh, Jalandhar, Bhubaneswar, Salem, Mira-Bhayandar, Warangal, Jalgaon, Kota, Bhiwandi, Saharanpur, Gorakhpur, Bikaner, Amravati, Noida, Jamshedpur, Bhilai, Cuttack, Firozabad, Kochi, Nellore, Bhavnagar, Dehradun, Durgapur, Asansol, Rourkela, Nanded, Kolhapur, Ajmer, Akola

 

 

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