Genes Diseases
    November 19, 2024

    Osteosarcoma: A cancer of the bone.

    What is the Osteosarcoma? Osteosarcoma is a type of bone cancer that primarily affects children…
    Genes Tests
    November 22, 2024

    Circulating Tumor Cells (CTCs)

    What is Circulating Tumor Cells (CTCs)? CTCs are fragments of tumor cells that have broken…
    200+ Genes Queries
    November 21, 2024

    How can genetic diseases impact the development and economic growth of countries?

    Genetic diseases can hinder the development and economic growth of countries by: Reducing productivity: Individuals…
    Genes Diseases
    November 18, 2024

    Familial Adenomatous Polyposis (FAP): A disorder increasing the risk of colon cancer.

    What is the Familial Adenomatous Polyposis (FAP)? Familial Adenomatous Polyposis (FAP) is a genetic condition…
    200+ Genes Queries
    November 20, 2024

    What are the unique challenges faced by individuals with genetic diseases in developing countries?

    Individuals with genetic diseases in developing countries face unique challenges, including: Limited access to healthcare:…
    200+ Genes Queries
    November 20, 2024

    What are the ethical considerations of genetic testing?

    ·  Privacy and confidentiality: Protecting the sensitive information obtained through genetic testing. ·  Informed consent:…
    Genes Tests
    November 22, 2024

    African Ancestry

    What is African Ancestry?  African ancestry testing, also known as DNA ancestry testing or genetic…
    200+ Genes Queries
    November 21, 2024

    What are the long-term implications of genetic diseases for aging?

    Genetic diseases can have significant long-term implications for aging, including: Increased risk of age-related conditions:…
    Genes Tests
    November 21, 2024

    Gaucher Disease Carrier Test

    What is Gaucher Disease Carrier Test ? A carrier test for Gaucher disease is a…

    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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