Seckel syndrome NGS panel Test Details:
Seckel syndrome panel (NGS Panel ATR, RBBP8, CENPJ, CEP152, CEP63, ATRIP)
What is Seckel syndrome NGS panel Test ?
Seckel syndrome NGS panel Test is a medical speciality that determines the cause and nature of diseases by examining and testing body tissues (EDTA blood or DNA). It is a Seckel syndrome NGS panel Test that screens of severe conditions.
Seckel syndrome, an autosomal recessive disorder, is the most common of the microcephalic osteoplastic dwarfisms. Seckel syndrome is characterized by proportionate dwarfism of prenatal onset, severe microcephaly with a bird-headed like appearance and mental retardation.
Haematological abnormalities with chromosome breakage have only been found in 15 to 25% of patients. The differential diagnosis with microcephalic osteoplastic dwarfism type II can only be made with a complete radiographic survey in the first years of life. Besides to a wide phenotypic heterogeneity between affected patients, genetic heterogeneity has also been proven, with three loci identified to date by homozygosity mapping.
Seckel syndrome is characterized by abnormally slow growth during fetal development (intrauterine growth retardation), resulting in low birth weight. Unusually slow growth (growth retardation and delayed bone maturation) continues after birth (postnatal) and typically leads to short stature (dwarfism) with proportional development of the arms and legs.
Besides, infants with Seckel syndrome have distinctive abnormalities of the head and facial (craniofacial) area. In most cases, affected infants may have microcephaly, a condition that indicates that the head circumference is smaller than would be expected for an infant’s age and sex.
Seckel syndrome is a rare disorder that is inherited as an autosomal recessive trait. Three variants of Seckel syndrome involve disruptions or changes (mutations) of genes on three different chromosomes. The gene map locations are Seckel syndrome 1, on chromosome 3, Seckel syndrome 2, on chromosome 18, and Seckel syndrome 3, on chromosome 14.
Treatment for Seckel Syndrome:
With the advent of technically superior ultrasonography, Seckel syndrome may be diagnosed before birth (prenatally). In fetal ultrasonography, reflected sound waves are used to create an image of the developing fetus. After delivery, Seckel syndrome may be suspected based upon thorough clinical evaluation, a detailed patient history, and a variety of specialized tests.
What type of sample are needed to do a Seckel syndrome NGS panel Test?
An EDTA blood or DNA for testing can be obtained from several bodily sources. The cells are the most commonly tested are derived.
Standard Biological Seckel syndrome NGS panel Test Samples: EDTA blood or DNA
How accurate is the Seckel syndrome NGS panel Test?
Seckel syndrome NGS panel Test is generally considered to be the most accurate testing method available. DNA Labs India’s Seckel syndrome NGS panel Test is regarded as a benchmark by most doctors. The most precise and precise Seckel syndrome NGS panel Test in India.
How many days does it take to obtain Seckel syndrome NGS panel Test results?
Results of Seckel syndrome NGS panel Test test are usually available from the laboratory within one week to 5 weeks.
For a standard Seckel syndrome NGS panel Test, DNA Labs India returns Seckel syndrome NGS panel Test results in 7 to 10 business days once all samples are received at the lab.
DNA Labs India understands that waiting for Seckel syndrome NGS panel 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 the Seckel syndrome NGS panel Test be done during pregnancy?
Prenatal Seckel syndrome NGS panel Test is a sensitive subject because of the ethical and legal issues involved, including the risks of an invasive test. It would help if you talked with your doctor.
How much does a Seckel syndrome NGS panel Test cost?
A standard Seckel syndrome NGS panel Test cost you 20000/- INR.
Why Choose DNA Labs India for Seckel syndrome NGS panel Test?
DNA labs India’s Seckel syndrome NGS panel Test follows with dual testing for 100% accuracy when determining a Seckel syndrome NGS panel Test.
- We are the leading lab for Seckel syndrome NGS panel 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 Seckel syndrome NGS panel Test?
You can either book online at the link provided. If you book and make the payment online free home collection service is offered to patients of all Seckel syndrome NGS panel Test.
How can I locate a Seckel syndrome NGS panel Test facility?
DNA labs India has 3000 plus sample collection centres across India for Seckel syndrome NGS panel Test.
You can choose the centre and book the Seckel syndrome NGS panel Test online. For all online bookings made and payment paid a free home sample collection service is provided.
List of Seckel syndrome NGS panel Test collection centres in India is 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.