Genetic tests are incomplete without appropriate advice and guidance. Genetic counselors need to frequently speak to the clients about complex scientific and emotional issues. The counseling involves –
• Confirming, diagnosing or ruling out a genetic condition.
• Communicating genetic risk for future generation.
• Providing psychological support.
Our highly qualified genetic counselors offer pre and post test counseling either online, by telephone, or in person.
For More Information and Booking Visit www.geneticcounseling.ae
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E3087 – Genetic Counseling Pre/Post, E3086 – Genetic Counseling Pre and Post, E3087 – Genetic Counseling Followup.
Fertility Profile0 out of 5
The profile provides a thorough evaluation that can identify many problems related to hormone imbalances that affect fertility. Early detection can help your patients address those issues and identify the need for more specialized care. Patients can collect their samples conveniently and at the appropriate cycle times with minimal disruption to their lives and busy work schedules. Sampling is done on days 3 and 21 of the menstrual cycle. Dried blood spot samples are collected on days 3 and 21 of the menstrual cycle, and saliva samples are collected only on day 21. The day 3 sample is optimal for assessment of ovarian reserves with the FSH and LH tests, while the other hormones are measured mid-luteal (day 21 commonly), when the level of hormones should be optimal for a successful pregnancy.
Heart Panel0 out of 5
The Heart Panel is a comprehensive 133 genetic diagnostic tool developed to cover a wide spectrum of cardiomyopathy and channelopathy diagnostics. Typically there is a difficulty to distinguish between the cardiomyopathy and channelopathy conditions and on some occasions the patient can actually have both. The Heart Panel provides a high-quality readout of all clinically relevant genes associated with both conditions. The OS-Seq™ technology provides high coverage clinical grade sequencing and enables reliable diagnostics for patients with significantly lower costs and faster turnaround time.
Note: Additional charges will apply for Deletion/Duplication Analysis
Comprehensive Stool Analysis0 out of 5
Many chronic disorders come from digestive problems and inadequate nutrient absorption. Proper gastrointestinal function is needed to eliminate toxic substances, pathogenic microbes, and undigested food particles from the body to prevent health problems. Nutrients require a specific internal environment to be properly digested and transported throughout the body.The comprehensive stool digestive analysis (CSDA) detects the presence of pathogenic microorganisms such as yeast, parasites, and bacteria that contribute to chronic illness and neurological dysfunction. It provides helpful information about prescription and natural products effective against specific strains detected in the sample.
Carrier Screening Test0 out of 5
Carrier screening analyzes 571 unique genes for mutations that are known to cause 210 genetic conditions encompassing more than 400 genetic diseases. The majority of the conditions included in Carrier Screening are inherited in an autosomal recessive pattern.
Diabetes/Obesity Panel0 out of 5
Diabetes is a group of not well-understood disorders characterized by abnormal glucose levels. As a complex disease, diabetes is the result of the interplay between the individual’s genetic make-up and the environment and there are multiple genes that are known to be associated with this condition; thus, a multigene panel represents a cost-effective option to identify the genetic cause of diabetes.
Sleep Balance Profile0 out of 5
When the master stress hormone cortisol is chronically elevated, particularly at night, it inhibits sleep and leads to lower melatonin levels. In addition to stress-related sleep disturbances, melatonin levels naturally die as we age – triggering further imbalances. The Sleep Balance Profile – the first four-point test offers a complete diurnal pattern of melatonin and cortisol to help patients struggling with hormone-related sleep imbalances.
Organic Acid Test0 out of 5
The Organic Acids Test (OAT) provides an accurate evaluation of intestinal yeast and bacteria. The test includes 74 urinary metabolite markers that can be very useful for discovering underlying causes of chronic illness such as behavior disorders, hyperactivity, movement disorders, fatigue and immune function. The cause of these high levels could include: oral antibiotic use, high sugar diets, immune deficiencies, and genetic factors. The OAT is strongly recommended as the initial screening test. The Microbial Organic Acids Test (MOAT) is ideal for follow-up to the OAT and is often recommended by practitioners looking for a specific abnormality, to monitor certain microbial imbalances, or to assess treatment efficacy.
Targeted Mutation Screening0 out of 5
The test identifies the mutated gene or genes causing a genetic disease in your family. The identification of a gene mutation(s) allows for further steps to be taken to prevent the passing on of the condition to future generations and may aid in the improvement of treatment of an affected individual.
Inherited Disease Panel0 out of 5
Broad genetic survey test for investigating general susceptibility and/or carrier condition for the included Mendelian disorders. 300 genes associated with >700 inherited diseases, including neuromuscular, metabolic, cardiovascular, and developmental diseases.
Pan Ethnic Carrier Screen0 out of 5
Pan Ethnic Carrier Screen is the most comprehensive genetic carrier screen for common diseases . It examines around 2000+ common mutations across 250+ genetic diseases, including Cystic Fibrosis, Sickle Cell Disease, Thalassemia, Spinal Muscular Atrophy, Tay-Sachs Disease. and Fragile X Syndrome. Many of the diseases included in the panel can shorten life expectancy and/or cause physical or cognitive impairment if left undiagnosed &/or untreated.