Genes Tests
    November 22, 2024

    Personalized Treatment

    What is Personalized Treatment?  Personalized treatment, also known as precision medicine, is a medical approach…
    Genes Tests
    November 22, 2024

    Human Identification

    What is Human Identification?  Human identification testing is a process used to determine the identity…
    Genes Treatments
    November 23, 2024

    Tecartus: Used to treat certain types of mantle cell lymphoma.

    Brief information about it: Tecartus is a chimeric antigen receptor (CAR) T-cell therapy used to…
    Genes Tests
    November 22, 2024

    UGT1A1 Testing (for irinotecan toxicity)

    What is UGT1A1 Testing?  UGT1A1 testing is a genetic test used to determine a person’s…
    200+ Genes Queries
    November 20, 2024

    How can genetic research contribute to personalized medicine?

    Genetic research is a key driver of personalized medicine, which aims to tailor medical treatments…
    Genes Tests
    November 22, 2024

    EGFR Testing (for lung cancer treatment)

    What is EGFR Testing?  EGFR (Epidermal Growth Factor Receptor) testing is a genetic test used…
    Genes Tests
    November 22, 2024

    Genetic Testing for Infertility

    What is Genetic Testing for Infertility?  Genetic testing for infertility is a medical procedure used…
    200+ Genes Queries
    November 21, 2024

    What are the ethical considerations of using genetic technologies to modify the genomes of future generations?

    The use of genetic editing technologies to modify the genomes of future generations raises significant…
    200+ Genes Queries
    November 20, 2024

    What is the genetic basis of muscular dystrophy?

    Muscular dystrophy is a group of genetic disorders that cause progressive muscle weakness and wasting.…

    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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