200+ Genes Queries
    November 20, 2024

    What is the genetic cause of phenylketonuria (PKU)?

    PKU is a genetic disorder caused by a mutation in the PAH gene, which is…
    Genes Diseases
    November 19, 2024

    Melanoma: A type of skin cancer.

    What is the Melanoma ? Melanoma is a type of skin cancer that develops in…
    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 Diseases
    November 19, 2024

    Cornelia de Lange Syndrome: A genetic disorder affecting growth, development, and facial features.

    What is the Cornelia de Lange Syndrome ?  Cornelia de Lange Syndrome (CdLS) is a…
    Genes Treatments
    November 23, 2024

    Levodopa/carbidopa: Used for Parkinson’s disease.

    Brief information about it: Levodopa/carbidopa is a combination medication used to treat Parkinson’s disease, a…
    Genes Tests
    November 21, 2024

    Phenylketonuria (PKU) Screening

    What is Phenylketonuria (PKU) Screening?  Phenylketonuria (PKU) screening is a mandatory test performed on newborns…
    Genes Treatments
    November 23, 2024

    Ceredase: Used for Gaucher disease.

    Brief information about it: Ceredase is an enzyme replacement therapy (ERT) used to treat Gaucher…
    Genes Treatments
    November 23, 2024

    Aldurazyme: Used for Hunter syndrome.

    Brief information about it: Aldurazyme is an enzyme replacement therapy (ERT) used to treat Hunter…
    Genes Diseases
    November 18, 2024

    Retinitis Pigmentosa: A progressive eye disorder causing night blindness and loss of peripheral vision.

    What is the Retinitis Pigmentosa ? Retinitis pigmentosa (RP) is a group of inherited eye…

    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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