Genes Tests
    November 22, 2024

    Lynch Syndrome Testing (for colorectal cancer risk)

    What is Lynch Syndrome Testing?  Lynch syndrome is a hereditary condition that increases the risk…
    Genes Diseases
    November 18, 2024

    Hereditary Nonpolyposis Colon Cancer (HNPCC): A disorder increasing the risk of colon cancer.

    What is the Hereditary Nonpolyposis Colon Cancer (HNPCC) ? HNPCC, also known as Lynch syndrome,…
    Genes Diseases
    November 19, 2024

    Multiple Myeloma: A cancer of the plasma cells.

    What is the Multiple Myeloma ? Multiple myeloma is a type of cancer that affects…
    Genes Tests
    November 21, 2024

    Non-invasive Prenatal Testing (NIPT)

    What is Non-invasive Prenatal Testing (NIPT) ? Carrier Testing is a genetic test to determine…
    Genes Treatments
    November 23, 2024

    AVXS-101: Being developed for spinal muscular atrophy (SMA).

    Brief information about it: AVXS-101, now known as Spinraza, is a gene therapy medication used…
    200+ Genes Queries
    November 21, 2024

    How can exposure to toxins and pollutants affect the risk of genetic diseases?

    Exposure to toxins and pollutants can increase the risk of developing genetic diseases by: Damaging…
    Genes Tests
    November 22, 2024

    Autism Spectrum Disorder Testing (for genetic risk factors)

    What is Autism Spectrum Disorder Testing?  ASD genetic testing is a specialized type of genetic…
    200+ Genes Queries
    November 20, 2024

    How can individuals protect their genetic privacy?

    Individuals can take steps to protect their genetic privacy, including: Understand genetic testing policies: Review…
    Genes Treatments
    November 25, 2024

    High cholesterol: Statins

    Brief information about it: Calcium channel blockers are a class of medications used to treat…

    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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