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By Mahek | Published on April 18, 2025

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Health / April 18, 2025

How to Spot and Manage Hemophilia Early

Hemophilia rarely enters the scene with flashing lights and alarms. More often, it creeps into childhood, so early diagnosis makes all the difference.

Today is World Hemophilia Day, and while it’s not the sort of date most people pencil into calendars, it should be. Because hidden behind the Latin-sounding syllables and medical mystique is a condition that’s both ancient and misunderstood.

If the body were a soundtrack, blood would be its rhythm section: steady, dependable, always showing up on cue. It flows, it nourishes, it seals the deal with a clot when you nick your finger slicing bread. Now imagine a life where blood doesn’t know when to stop. A skinned knee becomes an afternoon affair. A simple tooth extraction is a logistical nightmare. Welcome to the oddly invisible world of hemophilia.

What Exactly Is Hemophilia?

In simple terms, hemophilia is a genetic disorder where your blood forgets how to clot properly.

Says Dr. Tushar Rane, Internal Medicine Expert at Apollo Spectra Hospital in Mumbai, “Haemophilia is a genetic disorder where the blood lacks certain clotting factors, leading to prolonged bleeding. Even minor injuries can cause excessive blood loss, and internal bleeding may occur.”

There are two main types:

Hemophilia A, caused by a deficiency of clotting factor VIII

Hemophilia B, caused by a deficiency of clotting factor IX

Both sound as if they belong to an elaborate card trick, but they’re very real and crucial to the body’s emergency response system. Without these clotting factors, even a paper cut can overstay its welcome.

Hemophilia is an inherited condition, meaning it runs in families like curly hair or a fondness for pickle. It’s caused by a mutation in one of the genes responsible for producing clotting factors. The faulty gene is X-linked, which means it’s carried on the X chromosome. Since boys have only one X chromosome, they’re usually the ones who end up with the condition. Girls typically act as carriers, often unaware until they pass it along to a child. It’s one of those medical ironies: the mother carries the problem, but the son carries the consequences!

Symptoms Creep Up:

Hemophilia rarely enters the scene with flashing lights and alarms. More often, it creeps into childhood like a slightly off-colour crayon—not quite right, but not alarming enough to stop the drawing. According to Dr. Rane, “The symptoms include frequent nosebleeds, easy bruising, bleeding from cuts or injuries, joint swelling, and pain due to internal bleeding.” These might sound like typical playground injuries until you realize the bruises are unusually large, the nosebleeds last suspiciously long, and the child’s knee is swollen from what looked like a mild stumble.

Infants may show signs soon after birth, especially if there’s a family history.

“Timely diagnosis is key to managing hemophilia,” Dr. Rane adds. “It is often detected in infancy or early childhood through blood tests that check clotting factor levels. Parents might dismiss these signs, chalking it up to clumsiness or coincidence, but early attention could spare a child years of joint damage and chronic pain."

How to Diagnose it:

Testing for hemophilia is remarkably straightforward for something so life-altering. A simple blood test can measure clotting factor levels. If you have a family history of the condition, it's recommended to screen newborns shortly after birth. In many cases, diagnosis happens after a minor medical procedure (like circumcision or vaccination) leads to unexpected bleeding.

It’s worth noting that while hemophilia is rare, it's not rare enough. According to the World Federation of Hemophilia, over 400,000 people globally live with the condition, and many remain undiagnosed, especially in developing countries.

Can It Be Cured?

Sadly, no. Hemophilia is a lifelong condition. But it’s not a life sentence. With proper care, many people with hemophilia live long, full, and active lives. Treatment involves replacement therapy, where the missing clotting factor is injected into the bloodstream. In more advanced healthcare settings, this may be done prophylactically, meaning regularly scheduled doses are given to prevent bleeding episodes before they start.

“Apart from medical treatment, physical therapy and regular monitoring help maintain joint health and overall well-being,” says Dr. Rane. Joints take a beating in hemophilia, not from use, but from internal bleeds that can occur without any visible injury. Over time, these can lead to permanent damage unless managed with care.

Early Diagnosis Changes Everything:

Perhaps the most important message this World Hemophilia Day is this: recognition is power.

“Many parents are unaware that frequent bruising or prolonged bleeding in a child could be early signs of hemophilia,” warns Dr. Rane. While the condition itself cannot be reversed, early intervention can prevent serious complications... from joint destruction to dangerous internal bleeds.

With modern treatment options and increasing awareness, the days of hemophilia being a life-threatening mystery are behind us. Today, education, regular checkups, and accessible care are the tools that keep people with hemophilia safe, mobile and thriving.

Things Worth Remembering On World Hemophilia Days:

Hemophilia mostly affects boys but is carried by mothers.

It’s usually diagnosed in childhood.

Symptoms include unexplained bruises, frequent nosebleeds, joint pain, and prolonged bleeding.

Treatment exists and is effective, especially when started early.

It cannot be cured yet, but it can be managed beautifully.

So on World Hemophilia Day 2025, let’s raise awareness—not just in clinics and hospitals, but in living rooms, classrooms and playgroups.

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