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Seven people are diagnosed with cancer every minute in China, and cancer is all around you
Hereditary cancers are the dominant transmission of genes to the next generation. If one parent develops cancer due to genetic inheritance, there is a 1 in 2 chance that the child, whether male or female, will inherit the cancer gene, and may eventually develop the same cancer as the previous generation.
Women’s course 17 types of cancer
Men’s course 17 types of cancer
Fit for
Cancer patients
Someone in the family has cancer
Family members with early onset of cancer (age of onset< 50 years)
The same person in the family has multiple cancers
People with certain chronic diseases (e.g. pancreatitis, breast hyperplasia, etc.)
Carriers of cancer gene mutations in the family
Screening for mutated genes at an early stage of cancer detection is possible to detect cancer earlier than traditional testing, and to detect cancer early, and to treat and prevent it accordingly.
Fit for
Those who have recovered from cancer
There is a family history of the condition
People with insufficient immunity or chronic diseases
People with poor diet and lifestyle habits
People who regularly engage in activities in highly radioactive or polluted environments
The child is naughty? Not paying attention in class? Do your homework like fighting? Severe hyperactivity disorder can lead to violent behavior in children.
Assist parents to find the cause of hyperactivity disorder in their children, and know whether autism is caused by genetic problems as early as possible, so that doctors can provide timely treatment.
Understand the risk of developing autism in the next generation
Provides information on more than 600 other recessive genetic diseases for patients
Fit for
Medical testing for attention deficit/hyperactivity disorder requires identification of the cause
Couples with a family history of ADHD who need premarital or preconception genetic counseling
Couples who have given birth to a child with ADHD
Couples who have given birth to a child with ADHD
Children with distracted or difficult concentration, excessive activity, and weak self-management skills
Help the children from the stars as early as possible so that children with autism are no longer lonely
Assist parents to find the cause of their child’s autism, know whether autism is caused by genetic problems as early as possible, and let doctors provide timely treatment.
Understand the risk of developing autism in the next generation
Provides information on more than 600 other recessive genetic diseases for patients
Fit for
Patients who have been medically tested for autism and need to find out the cause
Patients with normal karyotype but suspected autism who need to be diagnosed, such as: social communication disorders, language communication disorders, repetitive stereotyped behaviors, intellectual abnormalities, paresthesias, and other behavioral abnormalities such as majority, distraction, irritability, aggression, or self-harm
Couples with a family history of autism who need premarital or preconception genetic counseling
Couples who have given birth to a child with autism
With more than 22,000 genes that manage and control various aspects of the body, scientists are constantly researching to unlock the genetic code and find answers to your personal health.
Health risks
– More than 6,000 health-related genetic diseases, such as cancer, cardiovascular disease, neurological diseases, etc
Reproductive health risks
– More than 1,000 diseases that can be passed on to the next generation, such as muscle dystrophy, intellectual disability, etc
Risk of drug sensitivities
– 340 drug reactions, including cancer and heart medications
Risk of stroke and heart disease
– Carrying a high-risk genotype increases the risk of stroke and heart disease
Fit for
People who are highly concerned about their personal health
People with a family history of the disease
All healthy people
More than 3,000 genetically related diseases are tested based on the symptoms provided by the client
Some cases have symptoms but are not diagnosed as a disease; In some cases, a disease is diagnosed after the onset of symptoms, but the cause cannot be found. These symptoms may be caused by mutations in one’s own genes, which may not be known through general examinations. Clinical whole-exome genetic testing to identify the relevant mutations can help identify the cause of the mutation for further diagnosis and treatment.
Fit for
Have been diagnosed with a disease but do not know the cause
Symptomatic but not diagnosed with a disease
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