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Diseases - NxGen MDx
https://nxgenmdx.com/answer-center/diseases
Learn all about the diseases that NxGen MDx screens for. Click on the links below to learn more about each disease and to download the disease fact sheet. Arthrogryposis, Mental Retardation, and Seizures. Ataxia with Vitamin E Deficiency. Autoimmune Polyglandular Syndrome Type 1. Autosomal Recessive Alport Syndrome. Autosomal Recessive Polycystic Kidney Disease. Carnitine Palmitoyltransferase IA Deficiency. Carnitine Palmitoyltransferase II Deficiency. CLN3-Related Neuronal Ceroid Lipofuscinosis. Megalen...
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Disease Thesaurus - NxGen MDx
https://nxgenmdx.com/answer-center/disease-thesaurus
Hyperinsulinemia Hypoglycemia Of Infancy. Persistent Hyperinsulinemia Hypoglycemia Of Infancy. Medium Chain Acyl-CoA Dehydrogenase Deficiency. Carnitine Deficiency Secondary To Medium-Chain Acyl-CoA Dehydrogenase Deficiency. Deficiency Of Medium-Chain Acyl-CoA Dehydrogenase. Short Chain Acyl-CoA Dehydrogenase Deficiency. Short Chain Acyl-CoA Dehydrogenase Deficiency. Short Chain Acyl-Coenzyme A Dehydrogenase Deficiency. Lipid-Storage Myopathy Secondary To Short-Chain Acyl-CoA Dehydrogenase Deficiency.
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Fragile X Syndrome Genetic Testing | NxGen MDx
https://nxgenmdx.com/lab-test/fragile-x
Fragile X Syndrome Genetic Testing. Fragile X Syndrome Genetic Testing. Fragile X Syndrome Genetic Testing. This condition affects approximately 1 in 4,000 males and 1 in 8,000 females. The majority of males with Fragile X Syndrome. Women are carriers. Fragile X Syndrome is found in all ethnic groups and can occur in families with no history of mental retardation or autism. I have no family history of Fragile X. Am I still at risk? How is the test performed? The Fragile X Syndrome Genetic Carrier Screeni...
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Dominant V.S. Recessive Genetics Diseases
https://nxgenmdx.com/answer-center/inheritance-factors
All individuals have 2 copies of every gene. A recessive genetic disease occurs when both copies of a particular gene are mutated. A person that has 1 (one) mutated copy of a gene and 1 (one) normal copy of that same gene is considered a “carrier” for that recessive genetic disease, however they are not affected by that disease. In order to be affected by a recessive genetic disease, you would need to have 2 (two) mutated copies of the same gene. Are carriers of a genetically. Test is right for you.
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Nick Fischer, Author at NxGen MDx
https://nxgenmdx.com/author/nfischer
This author has not yet filled in any details. So far Nick Fischer has created 3 blog entries. Saturday, October 3rd of 2015 will be the second annual Run Heidi Run! August 21st, 2015. Comments Off on Run Heidi Run! Cystic Fibrosis Month – Raising CF Awareness. Cystic Fibrosis Month – Raising CF Awareness. May 12th, 2015. Comments Off on Cystic Fibrosis Month – Raising CF Awareness. NxGen MDx Honored as a Michigan 50 Companies To Watch Awardee. NxGen MDx Honored as a Michigan 50 Companies To Watch Awardee.
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News & Articles - Genetic Laboratory | NxGen MDx
https://nxgenmdx.com/journal
September 14th, 2015. Comments Off on Oh Baby! Happy Newborn Screening Awareness month! Often heard of in the hospital or clinic as the PKU test , newborn screening is so much more. Depending upon the state a child is born in, newborn screening may screen for more than 60 different inherited genetic disorders. To determine the disorders screened for in your state, please visit baby’s first test. And how many babies does this equate to per year that are screened in the United States? August 21st, 2015.
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Common ICD Codes - NxGen MDx
https://nxgenmdx.com/answer-center/common-icd-codes
Family history of genetic disease carrier. Supervision of normal first pregnancy. Supervision of other normal pregnancy. Supervision of high-risk pregnancy with elderly primigravida. Supervision of high-risk pregnancy with elderly multigravida. Testing of female for genetic disease carrier status. Testing of male for genetic disease carrier status. Encounter for routine screening for malformation using ultrasonics. Other specified antenatal screening. Screening for cystic fibrosis. Factor V Leiden Testing.
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Universal Test Panel - Genetic Screening | NxGen MDx
https://nxgenmdx.com/lab-test/universal-test-panel
With over 99% accuracy, the Universal Test Panel. Is one of the world's most precise and thorough tests for detecting genetic markers for 22 of the most common genetic diseases that may affect pregnancy and future child development. If you and your partner are both carriers of the same recessive genetic disease, there is a 25% chance your child will inherit two copies of the abnormal gene and become affected by the genetic disease. 1 in 10 individuals are carriers. The Universal Test Panel. Anemia, low p...
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Factor V Leiden | NxGen MDx
https://nxgenmdx.com/lab-test/factor-v-leiden
Out of every 100. People in North America have Factor V Leiden. A condition that causes blood clotting, most often restricted to the veins. Clots can break off and travel to the lung, potentially causing pulmonary embolism. Symptoms include difficulty breathing, chest pain and palpitations. While it is rare for these clots to cause a stroke or heart attack, a transient ischemic attack, or mini-stroke , is more common. Caucasians are carriers for Factor V Leiden. How is the test performed? Are carriers of...
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Spinal Muscular Atrophy (SMA) Genetic Testing | NxGen MDx
https://nxgenmdx.com/lab-test/spinal-muscular-atrophy
Spinal Muscular Atrophy (SMA) Genetic Testing. Spinal Muscular Atrophy (SMA) Genetic Testing. Spinal Muscular Atrophy (SMA) Genetic Testing. A severe and often fatal genetic disorder, Spinal Muscular Atrophy (SMA). If both parents are carriers of an abnormal SMN1 gene, then there is a chance that each parent will pass the abnormal gene on to their child. Having two copies of the abnormal gene will result in a 1 in 4 (25%) chance that the child will have SMA. SMA frequency varies by ethnicity. 1 in 3,300.
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