Genes Tests
    November 22, 2024

    23andMe

    What is 23andMe?  23andMe provides DNA testing kits that you can purchase directly from their…
    Genes Tests
    November 21, 2024

    Amniocentesis

    What is Amniocentesis? Amniocentesis is a prenatal diagnostic procedure where a small sample of amniotic…
    200+ Genes Queries
    November 20, 2024

    What are the challenges and limitations of gene therapy?

    ·  Delivery challenges: Ensuring that the normal gene is delivered to the correct cells and…
    Genes Diseases
    November 19, 2024

    Skin Cancer: A cancer of the skin.

    What is the Skin Cancer? Skin cancer is a type of cancer that develops in…
    200+ Genes Queries
    November 21, 2024

    How can we balance the pursuit of scientific progress with the need to protect human rights and dignity?

    Balancing the pursuit of scientific progress with the need to protect human rights and dignity…
    Genes Diseases
    November 18, 2024

    Heart Disease: A group of conditions affecting the heart and blood vessels.

    What is the Heart Disease ? Heart disease, also known as cardiovascular disease, is a…
    Genes Tests
    November 21, 2024

    Inhibin-A Screening

    What is Inhibin-A Screening? Inhibin-A is a protein produced by the ovaries. It is used…
    Genes Tests
    November 22, 2024

    Whole Genome Sequencing

    What is Whole Genome Sequencing?  Whole Genome Sequencing (WGS) is a powerful genetic testing technique…
    Genes Diseases
    November 18, 2024

    Neurofibromatosis Type 2 (NF2): A disorder causing benign tumors to grow on the nerves and brain.

    What is the Neurofibromatosis Type 2 (NF2) ? Neurofibromatosis Type 2 (NF2) is a genetic…
    200+ Genes Queries
    November 20, 2024

    How can genetic research improve our understanding of disease?

    Genetic research has significantly advanced our understanding of diseases by: Identifying disease-causing genes: Identifying the…

    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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