Genes Tests
    November 22, 2024

    Genome-Wide Association Studies (GWAS)

    What is Genome-Wide Association Studies (GWAS)?  Genome-Wide Association Studies (GWAS) are large-scale genetic studies that…
    Genes Diseases
    November 18, 2024

    Arthritis: A joint inflammation disorder.

    What is the Arthritis ? Arthritis is a general term for conditions that cause inflammation…
    Genes Tests
    November 22, 2024

    Forensic Genealogy

    What is Forensic Genealogy?  Forensic genealogy is a relatively new field that applies genetic testing…
    Genes Diseases
    November 19, 2024

    Ewing Sarcoma: A cancer of the bone.

    What is the Ewing Sarcoma ? Ewing sarcoma is a rare type of bone cancer…
    200+ Genes Queries
    November 21, 2024

    How can we ensure that genetic services are accessible to people in all parts of the world?

    Ensuring that genetic services are accessible to people in all parts of the world requires:…
    200+ Genes Queries
    November 21, 2024

    What are the psychological and emotional effects of living with a genetic disease as a child?

    Living with a genetic disease as a child can have significant psychological and emotional effects,…
    Genes Diseases
    November 19, 2024

    Leukemia: A cancer of the blood-forming cells.

    What is the Leukemia ? Leukemia is a type of cancer that affects the blood…
    Genes Tests
    November 21, 2024

    Homocystinuria Screening

    What is Homocystinuria Screening?  Homocystinuria screening is a genetic test to detect a rare metabolic…
    Genes Tests
    November 22, 2024

    Multiple Sclerosis Testing (for genetic risk factors)

    What is Multiple Sclerosis Testing?  Multiple Sclerosis (MS) is a chronic autoimmune disease that affects…
    Genes Tests
    November 22, 2024

    Genetic Testing for Infertility

    What is Genetic Testing for Infertility?  Genetic testing for infertility is a medical procedure used…

    What is a Genes Disease ?

    A genes disease, often known as a genetic disorder, is a condition caused by abnormalities in an individual’s DNA. These abnormalities can occur in one or multiple genes and may be inherited from one or both parents, or they may develop as a new mutation. Genes are responsible for instructing cells on how to produce proteins, which are vital for bodily functions and growth. When there’s a mutation in a gene, it can disrupt this process, leading to genetic disorders.

    Common examples include cystic fibrosis, sickle cell anemia, and Huntington’s disease. Some genetic disorders are relatively rare, while others may affect millions of people worldwide. These conditions can lead to a range of health issues, from mild symptoms to serious complications. Research on genetic diseases is ongoing, with advances in genetic testing and gene therapy offering hope for improved diagnosis, management, and potential treatments for those affected.

    Genes Diseases Cure Video

    1 / 21 Videos
    1

    हंटिंगटन रोग में जीवन प्रत्याशा क्या होती है?

    01:00
    2

    सिकल सेल क्राइसिस के प्रमुख लक्षण क्या हैं?

    01:00
    3

    शिशुओं में हीमोफीलिया के लक्षण क्या होते हैं?

    00:43
    4

    कोशिका, गुणसूत्र, डीएनए और जीन बीच क्या संबंध है?

    02:00
    5

    हीमोफीलिया क्या है?

    00:50
    6

    डाउन सिंड्रोम होने के कारण क्या हैं?

    01:00
    7

    क्या Sickle Cell Anemia वंशानुगत है?

    01:00
    8

    clinical exome sequencing || clinical exome sequencing test information in hindi ||

    04:00
    9

    Fragile x syndrome disease information in hindi || symptoms, diagnosis and treatment of fragile x

    03:28
    10

    Evans Syndrome | इवांस सिंड्रोम कैसे होता है, इवांस सिंड्रोम में क्या खाएं,

    03:29
    11

    लिम्फोमा क्या है || lymphoma complete information in hindi for healthcare people

    06:31
    12

    Drug induced immune cytopenia | साइटोपेनिया क्या है, साइटोपेनियाके कारण, साइटोपेनिया का इलाज

    03:14
    13

    कोशिका क्या है?

    01:05
    14

    Fragile X syndrome का treatment और therapy क्या है?

    01:06
    15

    लड़कियों व लड़कों में Fragile X syndrome के लक्षण क्या होते हैं?

    00:39
    16

    हंटिंग्टन रोग क्या है?

    02:10
    17

    सिकल सेल एनीमिया का इलाज और उपचार क्या है?

    00:55
    18

    शिशुओं में हीमोफीलिया के लक्षण क्या होते हैं?

    00:43
    19

    क्या Sickle Cell Anemia वंशानुगत है?

    01:00
    20

    डीएनए क्या है? What is DNA?

    01:00
    21

    हंटिंगटन रोग में जीवन प्रत्याशा क्या होती है?

    01:00
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