+982188201760 +982188201761 +982188201762
Register
Login
فــا
موسسه پزشکی نسل امید
موسسه پزشکی نسل امید
If you are at the pre-marriage stage or before deciding to get pregnant or you are worried about your future pregnancy for any reason, our consultants at hope generation institute are beside you step by step. We carefully check your past medical history and family history. Our genetic counselors check the possibility of repeating risks in your future pregnancy and we will do the required clinical examination step by step to guarantee your future pregnancy health. Our goal is to provide the best services for supporting couples, particularly at-risk ones, to maintain maternal & fetal health. So, we also offer full-skilled specialists and up-to-date high-tech equipment in pre-pregnancy care and genetic services. Our pre-pregnancy services...
Services
If you are at any stage of your pregnancy, we are by your side as one of the leading providers of prenatal care and genetic services for pregnant women. Our clinical services are provided by full-skilled specialists certified by the International Fetal Medicine Foundation (FMF). Our main concern at Hope Generation Institute is maternal and fetal health. So, we use up-to-date four-dimensional ultrasound technology following international standards. Also, if you need invasive (amniocentesis and CVS) and non-invasive (NIPT) diagnostic tests during pregnancy, we provide these services by specialists who have a lot of experience in this field. Our expertise lies within all types of fetal medicine, giving you the best possible healthcare.
Services
We are trying to provide comprehensive professional services for future generation health. By timely diagnosis and treatment of metabolic disorders in newborns, we can significantly prevent future disabilities and more neonatal complications. In this regard, Hope Generation Institute, as known medical institute, has a well-equipped and international standard set up to diagnose and treat congenital metabolic diseases. Also, if your future pregnancy is at-risk for metabolic diseases, you can use our prenatal diagnosis (PGD) service. We provide " newborn hereditary metabolic disorder screening" services in a supportive and reliable environment, with the cooperation of experienced specialists and using the most advanced related technologies
Services
About Image
About Image
shapes
shapes
shapes
about Image

Calculation of gestational age

To calculate the gestational age and possible delivery date, enter the date of the first day of your last menstrual period by day, month and year in the box below.

Computing
Service Centers

Services

Online consultation Online Reservation

Genetic counselling services play an essential role in fetal and neonatal health by considering the prevalence risk of disabilities in a family.
Your genetic counsellor considers the possible risk of disease occurrence in which genetics plays an important role. Genetic counselling is a way for people to understand how genetic illnesses can affect them and their family.

Genetic counselling is the first level of our services at Hope Generation Institute. You can find our full-experience genetic counsellors who provide you with online personalized consulting at your "Profile".

Book an appointment today by clicking on the bellow “Request Registration " button.😊

Request registration

If you are applying for an online reservation at Hope Generation Institute, you can easily enter the relevant page by clicking the bellow "Registration"  button. 

On this page, by filling in Personal Identifiable Information, you can choose the service you want, which is a subset of one of the three centers of Hope Generation Institute. Then, choose your desired date and time from the displayed timetable.
If your information is registered correctly, a “Profile” will be automatically created for you, and the username and password will be sent to you via SMS and email.
Now, you can track all your services from your “Profile”. 


On the other hand, our colleagues will interact with you directly. if your selected service, needs to pay for the final reservation, you should do the electronic payment.
Otherwise, a message will be sent to you:

"Temporary reservation for the selected date and time has been successfully registered“

Please do not forget that the final registration of your time will be done after our colleagues' confirmatory call. So, we will contact you as soon as possible.


Book An Appointment Today …😊

Request registration

Vice President of Research

Fetal Growth and Development Disorders Research Center
hope plan

This project is carried out in 5 stages and its final goal is to identify the reservoir of mutations of common genetic diseases in the country. In the first phase, 1,500 ...

Gene Therapy and Regenerative Medicine Research Center
Contingent-NIPT Country plan

Recently, a new screening method called NIPT (Cell Free Fetal DNA Testing), which is based on the use of free fetal DNA in the mother's blood circulation, has been introd...

Person-centered medical research center and genometabolomics
National screening plan for hereditary metabolic diseases

hereditary metabolic disorders National Project: Currently, 10 laboratories in IRAN have the ability to perform standard metabolic tests. Hope generation institute passed...

About Image

Common Questions

Lethargy, laxity, whining, restlessness, frequent vomiting, weak sucking milk, weakness, difficulty in healing or breathing hard, seizures, difficulty in developmental skills in the child such as holding, laughing, rolling, sitting and etc.

It means the result of the screening test (newborn heel stick test) is positive, the confirmatory tests do not confirm the result and the baby hasn't related signs or symptoms. Actually, several conditions such as childbirth stress, infections during birth, mother use of antibiotics during pregnancy newborn use of antibiotics and etc., can cause a false positive result.

Lethargy, laxity and whining, restlessness, frequent vomiting in the child, not feeding well, poor sucking in the child, breathing disorder or difficulty breathing, seizures, delay in acquiring developmental skills in the child such as holding the neck, laughing, rolling, sitting and...

Click if you have any questions More

If there is a person suffering from hereditary and genetic disorders in the family, priority should be given to testing, and examining the affected person himself, and in the next step, if the affected person is not available, check the mandatory carriers or parents. The affected person (in cases of suspected autosomal recessive disorders or diseases caused by consanguineous marriage). Examining people based on the genealogy of possible disease carriers faces limitations and is not recommended.

 Genetic testing should be done after genetic counseling. In the course of the discussion, it will be determined whether such an experiment is necessary or not. In general, if genetic testing is necessary for an individual or a family, it is better to do it as soon as possible. For example, if the couple has visited before marriage, doing it at that time has priority over doing it after marriage. On the other hand, despite being informed about all aspects, some families sometimes postpone the investigations according to their opinion and choice until after marriage. However, if necessary, genetic tests must be done before pregnancy. If a family has not done these tests at the mentioned times for any reason, it is still better to do these tests as soon as possible (even in the early weeks of pregnancy).

Before trying to get pregnant, Specialist genetic counseling is recommended with the documents of sick people in the presence of couples. First of all, we should know that mental retardation has different causes, these causes are divided into two main groups, genetic and non-genetic, and their genetic causes are very diverse. It has a family in the affected person. As a result, genetic counseling is recommended before trying to get pregnant. In this consultation, after drawing a genealogy and taking a detailed history, the analysis of the genealogy information is done by a geneticist, and the probability of recurrence of this disease in the family is calculated based on the analysis and analysis of the genealogy, and since the causes of this The disease is different, the necessary genetic tests in the affected person are described in the order of importance, mentioning their benefits and limitations, and the appropriate steps based on the test results for the couple. So that the family can take action if they wish

Click if you have any questions More
Contingent first-trimester screening for aneuploidies with cell-free DNA in a Danish clinical setting
01/01/2023

Contingent first-trimester screening for aneuploidies with cell-free DNA in...

The primary aim of this study was to compare the screening performance for trisomy 21 (T21) between combined first-trimester screening (cFTS) with referral for invasive testing at a T21 risk ≥ 1 in 300, and contingent screening consisting of referral for invasive testing at a cFTS-T21 risk ≥ 1 in 100 and referral for cell-free DNA (cfDNA) testing at a cFTS-T21 risk between 1 in 100 and 1 in 1000. Secondary aims were to compare the incidence of fetuses diagnosed with trisomy 18 (T18), trisomy 13 (T13) or sex chromosome aneuploidy, and examine the association between fetal fraction of cfDNA in maternal blood and maternal/fetal characteristics.
The consequences of implementing non‑invasive prenatal testing with cell‑free fetal DNA for the detection of Down syndrome in the Spanish National Health Service: a cost-effectiveness analysis
01/01/2023

The consequences of implementing non‑invasive prenatal testing with cell‑fr...

DNA-based non-invasive prenatal testing (NIPT) using maternal blood constitutes an emerging technology for the detection of Down syndrome (DS). The aim of the study was to conduct a cost-effectiveness analysis to evaluate the economic costs and health implications of the introduction of NIPT based on cell-free fetal DNA analysis through different screening strategies for the detection of DS.
More
Presenting the results of the National Contingent-NIPT project at the official meeting of the Iran Academy of Medical Sciences
09/03/2023

Presenting the results of the National Contingent-NIPT project at the official meeting of the Iran Academy of Medical Sciences

The national plan "determining the use of NIPT test in the screening of chromosomal abnormalities in the first trimester of pregnancy based on the Contingent protocol using the Reflex DNA Testing method" was completed in September 1401. The implementers of the project in line with the advancement of the goals of this national plan and after holding numerous meetings and negotiations and collecting the opinions of professors, experts and health trustees of the country, including Mr. Dr. Malek Afzali, representatives of the Ministry of Health and Medical Education, representatives of forensic medicine and also the country's medical system organization in a meeting that was held on December 21 and hosted by the Academy of Medical Sciences discussed the results of this plan with the professors and scholars of the field. They paid health.
The importance and necessity of holding the placenta and fetus autopsy conference
08/10/2022

The importance and necessity of holding the placenta and fetus autopsy conference

In this meeting, which was held under the management of Dr. Madbari, the CEO of Hope Generation Medical Institute, specialists and experts from related fields expressed their views regarding the title of this conference. During this meeting, it was suggested to pay attention to the role of fetal autopsy in the diagnosis and management of pregnancies exposed to genetic disorders
More
Counseling and Genetic Diagnosis of Spinal Muscular Atrophy
15/08/2022

Counseling and Genetic Diagnosis of Spinal Muscular Atrophy

This disease is known as one of the most common genetic diseases with autosomal recessive inheritance and also the most common monogenic cause of early infant death. In this disease, the motor neurons of the anterior horn of the spinal cord and the base of the brain (Pons) are depleted and the affected person has difficulty in performing some voluntary movements. The probability of an individual being a carrier for SMA has been reported to be 1 in 25 to 50 in various populations. Studies conducted in our country have reported the number of carriers to be around 1 in 20 people, which is more common than other populations and shows the necessity of screening people in order to identify the carriers of this disease.
More

Gallery

  • All
  • Video and Animation
  • Image
  • Podcast
  • Pamphlet
know more

Center of Prevention & Treatment of Hereditary Metabolic Disorders

This center is a comprehensive and well-equipped center to prevent, diagnose and treat congenital metabolic diseases. Although each of the hereditary metabolic disorders is rare, according to global statistics, they have a high prevalence of about 1 in every 1500 live births, which is more common due to consanguineous marriages in our country. This category of diseases has non-specific symptoms and its symptoms can appear at any age from infancy to adulthood acutely or chronically. In this center, we aim to significantly reduce neonatal disabilities and deaths through timely diagnosis and treatment of metabolic disorders if possible, and prevent the occurrence of hereditary metabolic diseases in future pregnancies with prenatal diagnostic tests (PND & PGD).

know more
/uploads/services/balini.jpg
Department of Clinical Diagnosis

Based on the urgent need for a comprehensive and well-equipped center for t...

/uploads/services/MLT.png
Department of Diagnostic Laboratory

Global statistics show that one out of every 1,500 live births has metaboli...

Center of Genetics

Hope Generation Comprehensive Genetics Center is one of the most advanced medical genetics centers in the country. Genetic counseling and examination is one of the most important elements that help in the diagnosis and prevention of congenital anomalies. Therefore, this institute operates in the form of a comprehensive genetics center with the use of advanced global technologies. This center provides specialized services such as genetic counseling, prenatal diagnosis (PND) and preimplantation genetic diagnosis (PGD) of genetic diseases. With new molecular cytogenetic methods, this center is able to quickly detect chromosomal abnormalities on placental villi and amniotic fluid samples within 1 to 2 working days. Also, in this center, the products of pregnancy are examined in terms of pathology (autopsy) and genetics with the cooperation of geneticists and pathologists. In this institution, a comprehensive diagnostic approach to mental retardation, movement problems and congenital anomalies is carried out using modern genomic techniques.

know more
/uploads/services/Center of Genetics/www.iranfmf.ir-Center-of-Genetics--pic5.jpg
Department of Molecular Genetics

Our specialists and experts in the molecular genetics department provide a ...

/uploads/services/Center of Genetics/www.iranfmf.ir-Center-of-Genetics--pic4.jpg
Department of Next Generation Sequencing (NGS)

With the successful launch of Next Generation Sequencing-NGS methods in the...

/uploads/services/Center of Genetics/www.iranfmf.ir-Center-of-Genetics--pic9.jpg
Department of Molecular Cytogenetics

The molecular cytogenetic department of Hope Generation Medical Institute o...

/uploads/services/Center of Genetics/02.jpg
Department of Medical Cytogenetics

Our specialists and experts in this department examine the status of all ch...