200+ Genes Queries
    November 20, 2024

    What are the common methods used to diagnose genetic diseases?

    ·  Family history: Assessing the occurrence of similar diseases in relatives can provide clues about…
    200+ Genes Queries
    November 21, 2024

    What are the options available for couples at risk of having a child with a genetic disease?

    Couples at risk of having a child with a genetic disease have several options, including:…
    Genes Diseases
    November 18, 2024

    Hemochromatosis: A disorder causing iron overload.

    What is the Hemochromatosis? Hemochromatosis is a genetic disorder that causes the body to absorb…
    Genes Diseases
    November 18, 2024

    Retinoblastoma: A cancer of the eye.

    What is the Retinoblastoma ? Retinoblastoma is a rare type of eye cancer that affects…
    200+ Genes Queries
    November 20, 2024

    What are the privacy concerns associated with genetic testing?

    Genetic testing raises significant privacy concerns due to the sensitive nature of the information collected.…
    Genes Tests
    November 21, 2024

    Phenylketonuria (PKU) Screening

    What is Phenylketonuria (PKU) Screening?  Phenylketonuria (PKU) screening is a mandatory test performed on newborns…
    Genes Tests
    November 22, 2024

    African Ancestry

    What is African Ancestry?  African ancestry testing, also known as DNA ancestry testing or genetic…
    Genes Diseases
    November 18, 2024

    Ulcerative Colitis: An inflammatory bowel disease.

    What is the Ulcerative Colitis ? Ulcerative colitis (UC) is a chronic inflammatory bowel disease…
    Genes Tests
    November 22, 2024

    Alzheimer’s Disease Testing (for genetic risk factors)

    What is Alzheimer’s Disease Testing?  Alzheimer’s disease testing involves genetic analysis to identify individuals who…
    Genes Diseases
    November 19, 2024

    Tyrosinemia: A metabolic disorder affecting the metabolism of amino acids.

    What is the Tyrosinemia ?  Tyrosinemia is a rare genetic disorder that affects the way…

    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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