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https://www.mayoclinic.org/diseases-conditions/hemophilia/symptoms-causes/syc-20373327
https://www.pronto.com/shopping?qo=semQuery&ad=semA&q=hemophilia%20informations&o=758076&ag=fw&an=msn_s&rch=us259

https://ghr.nlm.nih.gov/condition/hemophilia

https://sites.google.com/site/geneticsprojecthemophilia/genotype

http://topics.medicinenet.com/topic/2/Hemophilia+Treatment+Options/?utm_campaign=8n1v352&utm_term=hemophilia%20advice&utm_medium=b&g_ti=kwd-78271586397028:loc-190&g_de=c&g_ci=287232350&g_ai=1252343871267881&utm_content=1&k=hemophilia%20information

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Mayo Clinic on E Mayo Blvd

Psychiatric Hospital

· Open

5779 E Mayo Blvd, Phoenix, AZ · (480) 301-8000
https://stepsforliving.hemophilia.org/basics-of-bleeding-disorders/hemophilia-treatment-centers

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My advice for the parent is to be overly protective so that your child wont get badly injured or even pass away
You should look fro treatment so that your child can be helped even though he has a deadly disease that has no cure.
Get ready if something were to happen for any reason.

My advice on having another child is not to because they are going to live a harsh life, but if you want another child go ahead and have one even though the possibility of your child inheriting the disease is pretty high.

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Hemophilia is passed down from mother to son. It is extremely

rare for a woman to have hemophilia. It is necessary, though, for a woman to be a carrier of the disorder for her son to acquire this disorder. Females have two X chromosomes whereas males only have one. When a boy is born, he takes one X chromosome from his mother and one Y chromosome from his father. Therefore, he can only get hemophilia through his mother.

Example One:

Mother(Carrier)+Father(Non-Affected)=50% chance of their son acquiring the disorder and 50% chance of their daughter being a

carrier.

Example Two:

Mother(Non-Affected)+Father(Hemophiliac)=All sons will be non-affected and all daughters will be carriers.

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Several different types of clotting factors are associated with different varieties of hemophilia. The main treatment for severe hemophilia involves receiving replacement of the specific clotting factor that you need, through a tube placed in a vein.

This replacement therapy can be given to combat a bleeding episode that's in progress. It can also be administered on a regular schedule at home to help prevent bleeding episodes. Some people receive continuous replacement therapy.

Replacement clotting factor can be made from donated blood. Similar products, called recombinant clotting factors, aren't made from human blood.

Other therapies may include:

Desmopressin (DDAVP). In mild hemophilia, this hormone can stimulate your body to release more clotting factor. It can be injected slowly into a vein or provided as a nasal spray.

Clot-preserving medications (anti-fibrinolytics. These medications help prevent clots from breaking down.

Fibrin sealants. These medications can be applied directly to wound sites to promote clotting and healing. Fibrin sealants are especially useful in dental therapy.

Physical therapy. It can ease signs and symptoms if internal bleeding has damaged your joints. If internal bleeding has caused severe damage, you may need surgery.

First aid for minor cuts. Using pressure and a bandage will generally take care of the bleeding. For small areas of bleeding beneath the skin, use an ice pack. Ice pops can be used to slow down minor bleeding in the mouth.

Vaccinations. Although blood products are screened, it's still possible for people who rely on them to contract diseases. If you have hemophilia, consider receiving immunization against hepatitis A and B.

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When you bleed, your body normally pools blood cells together to form a clot to stop the bleeding. The clotting process is encouraged by certain blood particles. Hemophilia occurs when you have a deficiency in one of these clotting factors.

There are several types of hemophilia, and most forms are inherited. However, about 30 percent of people with hemophilia have no family history of the disorder. In these people, an unexpected change (spontaneous mutation) occurs in one of the genes associated with hemophilia.

Acquired hemophilia is a rare variety of the condition that occurs when a person's immune system attacks clotting factors in the blood. It can be associated with:

Pregnancy

Autoimmune conditions

Cancer

Multiple sclerosis

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Hemophilia is a rare disorder in which your blood doesn't clot normally because it lacks sufficient blood-clotting proteins (clotting factors). If you have hemophilia, you may bleed for a longer time after an injury than you would if your blood clotted normally.

Small cuts usually aren't much of a problem. The greater health concern is deep bleeding inside your body, especially in your knees, ankles and elbows. That internal bleeding can damage your organs and tissues, and may be life-threatening.

Hemophilia is an inherited (genetic) disorder. Treatment includes regular replacement of the specific clotting factor that is reduced.

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A simple bump on the head can cause bleeding into the brain for some people who have severe hemophilia. This rarely happens, but it's one of the most serious complications that can occur. Signs and symptoms include:

Painful, prolonged headache

Repeated vomiting

Sleepiness or lethargy

Double vision

Sudden weakness or clumsiness

Convulsions or seizures

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Unexplained and excessive bleeding from cuts or injuries, or after surgery or dental work

Many large or deep bruises

Unusual bleeding after vaccinations

Pain, swelling or tightness in your joints

Blood in your urine or stool

Nosebleeds without a known cause

In infants, unexplained irritability

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Children with Hemophilia presented by The Delaware Valley Chapter of the National Hemophilia Foundation