200+ Genes Queries
    November 21, 2024

    Tay-Sachs Disease Carrier Test

    What is Tay-Sachs Disease Carrier Test ? A Tay-Sachs disease carrier test is a genetic…
    Genes Treatments
    November 23, 2024

    Panchakarma: A detoxification process that can help eliminate toxins and restore balance in the body.

    Brief information about it: Panchakarma is a comprehensive Ayurvedic detoxification process that involves five specific…
    Genes Diseases
    November 19, 2024

    Maple Syrup Urine Disease: A metabolic disorder affecting the breakdown of amino acids.

    What is the Maple Syrup Urine Disease ?  Maple named for the distinctive maple syrup-like…
    Genes Tests
    November 21, 2024

    Canavan Disease Carrier Test

    What is Canavan Disease Carrier Test ? The Canavan Disease Carrier Test is a genetic…
    Genes Tests
    November 21, 2024

    Cystic Fibrosis Screening

    What is Cystic Fibrosis Screening?  Cystic Fibrosis (CF) screening is a genetic test used to…
    Genes Diseases
    November 20, 2024

    Laryngeal Cancer: A cancer of the larynx.

    What is the Laryngeal Cancer ?  Laryngeal cancer, also known as throat cancer, is a…
    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:…
    Genes Diseases
    November 19, 2024

    Lymphoma: A cancer of the lymphatic system.

    What is the Lymphoma? Lymphoma is a type of cancer that affects the lymphatic system,…
    200+ Genes Queries
    November 21, 2024

    How can we ensure that the benefits of genetic research are shared equitably across generations?

    Ensuring that the benefits of genetic research are shared equitably across generations requires: International cooperation:…

    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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