Stem cell preservation is the process of collecting, processing, and storing stem cells from sources like umbilical cord blood and tissue for potential future medical treatments
INNOVIA BioBank offers cutting-edge facilities, certified and accredited operations, and a pioneering role in stem cell therapy and regenerative medicine in the MENA region.
Stem cells are collected non-invasively at the time of birth and stored in highly secure and controlled conditions to maintain their viability and integrity
Preserved stem cells have the potential to treat a wide range of conditions, including certain cancers, blood disorders, and genetic diseases, with ongoing research expanding their therapeutic potential
BabyCord Stem Cell Bank, a division of INNOVIA BioBank, specializes in the collection, processing, and long-term storage of umbilical cord blood and dental pulp stem cells, ensuring high-quality and secure preservation.
Yes, preserved stem cells can potentially be used for family members, subject to compatibility and the specific medical condition being treated.
Costs vary based on the type of preservation service chosen. INNOVIA BioBank offers various packages tailored to meet different needs and budgets, ensuring accessibility to this vital service.
With proper storage conditions, stem cells can be preserved for many years, potentially up to several decades, while maintaining their viability for future therapeutic use.
PGT-SR is a specialized IVF procedure used to identify embryos with the correct balance of genetic material, particularly beneficial for couples with chromosomal rearrangements. It's aimed at those who want to increase their chances of a healthy pregnancy by selecting embryos without structural genetic issues.
By selecting embryos that are free from specific structural genetic rearrangements, PGT-SR reduces the likelihood of miscarriages and unsuccessful pregnancies, as these conditions are often linked to genetic imbalances.
PGT-M tests embryos for specific genetic disorders before implantation, allowing couples at risk of passing on genetic conditions to select embryos free from those disorders.
Couples with a known risk of transmitting genetic conditions to their offspring should consider PGT-M as it offers a chance to ensure the health of their future children by preventing the inheritance of targeted genetic abnormalities
WES is a genetic test that examines all the exons in your genome, which are responsible for coding proteins. It can uncover the hidden causes of rare and inherited diseases, aiding in accurate diagnoses and personalized treatment plans.
Individuals with undiagnosed genetic conditions, families seeking insights into inherited diseases, and healthcare providers looking for detailed genetic information to inform treatment and family planning decisions can all benefit from WES.
WGS provides a comprehensive map of an individual's entire genetic makeup, offering insights into genetic predispositions, potential inherited conditions, and opportunities for personalized medicine.
By identifying genetic variations and mutations, WGS enables early detection of diseases, targeted treatment plans, and informed decisions on family planning, significantly advancing personalized healthcare.
Chromosomal Microarray is a genetic test that scans the genome for thousands of genetic abnormalities, such as deletions and duplications, providing a comprehensive view of an individual's genetic makeup and enabling accurate diagnosis of a wide range of genetic disorders.
By pinpointing specific genetic anomalies, CMA guides personalized medical care, helping clinicians make informed decisions on the treatment and management of various conditions, and improving outcomes for patients with genetic disorders.
Led by experienced clinical geneticists, our clinic specializes in diagnosing and managing genetic disorders, offering genetic testing, personalized treatment plans, and comprehensive care to support affected individuals and families.
Our clinic provides expert care designed to address the unique genetic needs of each patient, facilitating informed health management decisions in a supportive environment.
Our clinic offers both virtual and on-site personalized guidance and support for navigating genetic conditions, including risk assessment, genetic testing interpretation, and emotional support in a compassionate environment
With flexibility and convenience in mind, we provide tailored consultations to meet the specific needs of individuals and families dealing with genetic conditions, ensuring comprehensive care.
This test analyzes vaginal fluid or endometrial biopsy samples to identify the balance of bacteria, helping to detect conditions that might affect fertility, such as chronic endometriosis or recurrent implantation failure
Women experiencing fertility issues or recurrent pregnancy loss may benefit from this test, as it provides insights that can guide better care and treatment options.
This test is designed to determine the best time for embryo transfer by assessing if the uterine lining is receptive, improving the chances of successful implantation and pregnancy
Individuals or couples undergoing IVF treatments may consider this test to increase their chances of success by ensuring that embryo transfer is timed with optimal endometrial receptivity.
PGT-A stands for Preimplantation Genetic Testing for Aneuploidy, a process used in conjunction with IVF (In Vitro Fertilization) to increase the likelihood of a successful pregnancy. It involves screening embryos for aneuploidy - a condition where there are missing or extra chromosomes - before they are transferred to the uterus. This helps in selecting embryos with the best chance of developing into a healthy pregnancy, by avoiding those with chromosomal abnormalities that could lead to miscarriage or genetic disorders.
PGT-A is recommended for individuals or couples undergoing IVF who want to improve their chances of a successful pregnancy, reduce the risk of miscarriage, and avoid genetic disorders associated with chromosomal abnormalities. It is particularly beneficial for older women, those with a history of recurrent miscarriages, failed IVF cycles, or genetic disorders in the family. By supporting the strategy of single embryo transfer, PGT-A helps in achieving high pregnancy rates while minimizing the risks of multiple pregnancies and their associated complications.