cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion DNA test lab cost 26000.00 /- Rs

cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion DNA Test

cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion

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Reporting Time: 2 Week
Test Cost: 26000.00 /- Rs
Sample Type: 10 ML in Streck tube
cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test Description cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion 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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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 Microdeletion Rarity Common Symptoms
Syndrome
DiGeorge syndrome 1/2000 to -          congenital heart defect
Jan-00 -          cognitive impairments; below borderline normal IQ
  -          autoimmune disorder, etc.
1p36 deletion syndrome 1/5000 to -          development delay in growth and learning
1/10000 ability
  -          feeding difficulties, etc.
Williams syndrome 1/7500 to -          delay development of motor skills
1/20000 -          heart murmur, etc.
Koolen-de Vries syndrome 1/16000 -          feeding difficulties
-          heart defect
-          kidney or urological anomalies, etc.
Prader-Willi syndrome 1/15000 -          poor muscle tone
-          lack of eye coordination, etc.
Angelman syndrome 1/12000 to -          delayed development
1/20000 -          intellectual disability
  -          speech impairment
  -          problems with movement and balance (ataxia) , etc.
Smith-Magenis syndrome 1/15000 to -          mild to moderate intellectual disability
1/25000 -          delayed speech and language skills
  -          distinctive facial features, etc.
Cri-du-Chat syndrome 1/20000 to -          severe cognitive, speech, and motor delays
1/50000 -          small head size (microcephaly) , etc.
18q deletion syndrome 1/40000 -          mild to severe intellectual disability
-          mild to severe delayed development, etc.
Wolf-Hirschhorn syndrome 1/50000 -          distinctive facial features
-          delayed growth and development , etc.
Alagille syndrome 1/70000 to -          affect the development of heart, liver, kidney,
1/100000 and other system in the body
  -          poor weight gain and growth, etc.
Jacobsen syndrome 1/100000 -          delayed development
-          bleeding disorder
-          heart defects and congenital heart disease
-          kidney defects, etc.
Hereditary Neuropathy with 2-5/100000 -          affects peripheral nerves
Liability to Pressure Palsy (HNPP) -          loss of muscle function , etc.
Rubinstein-Taybi syndrome 1/100000 to -          short stature
1/125000 -          moderate to severe intellectual disability
  -          eye abnormalities, heart and kidney defects, dental problems, obesity , etc.
WAGR syndrome 1/500000 to -          aniridia, an absence of the colored part of the
1/1000000 eye
  -          reduction in the sharpness of vision (visual acuity) and increased sensitivity to light (photophobia)
  -          intellectual disability , etc.
Potocki-Shaffer syndrome Less than -          affects development of the bones, brain, and
100 case in the world other organs
  -          intellectual disability, delayed development of speech, motor skills (such as sitting and walking), and social skills , etc.
Miller-Dieker syndrome Less than -          abnormal brain development (lissencephaly)
1/100000 -          severe intellectual disability
  -          developmental delay
  -          weak muscle tone , etc.
1q21.1 deletion syndrome Less than -                       developmental delays
100 case in the world -                       mild-to-moderate intellectual disability
  -                       microcephaly, etc.
Kleefstra syndrome Less than -                       severely limited or absent speech
200 case in the world -                       weak muscle tone
  -                       heart defects
  -                       respiratory infections , etc.
Phelan-Mcdermid syndrome Less than -                       moderate to profound intellectual disability
1000 case in the world -                       absent or delayed speech
  -                       autism or autistic-like behavior, etc.

Cost of cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Test in India

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cellfree Noninvasive Prenatal Testing NIPT Plus Microdeletion Cost

₹ 26000.00
₹ 26000.00
₹ 26000.00
₹ 26000.00
₹ 26000.00
₹ 26000.00
₹ 26000.00