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Many people may not have heard of the disease.

But for some families, haemophilia

Is a condition that unknowingly passes from generation to generation.

.

Hemophilia is a bleeding disease, easy to stop, difficult to stop.

Caused by a gene abnormality on the X chromosome.

Causing the body to make proteins that do not help with blood clotting enough.

.

Patients are therefore at risk of bleeding longer than usual.

Or bleeding inside the joints and muscles.

.

Interestingly, many women may be carriers without symptoms.

But this abnormal gene can be passed on to the baby.

Especially a son who is more likely to show signs of the disease.

.

Screening before childbirth

So it's another important way to help family planning.

Reduce the risk of passing genetic diseases to future children.

.

# Hemophilia # Hemophilia # Genetic diseases

# Genetic test # Plan to have children

5 days agoEdited to

... Read moreจากประสบการณ์ส่วนตัวของผู้ที่มีคนในครอบครัวเป็นโรคฮีโมฟีเลีย ต้องบอกว่าโรคนี้สร้างความวิตกกังวลไม่น้อยกับคนในครอบครัว เนื่องจากเป็นโรคเลือดที่มีลักษณะเฉพาะคือเลือดออกง่ายและหยุดยาก ซึ่งถ้าไม่ระวังก็อาจทำให้เกิดภาวะแทรกซ้อนเช่นเลือดออกในข้อหรือกล้ามเนื้อได้ สิ่งที่สำคัญมากที่ผมได้เรียนรู้คือผู้ป่วยหญิงจำนวนมากอาจเป็นเพียงพาหะที่ไม่แสดงอาการ แต่สามารถส่งต่อยีนผิดปกตินี้ให้ลูกชาย ซึ่งอาจมีอาการรุนแรงกว่า ด้วยเหตุนี้การตรวจคัดกรองทางพันธุกรรมก่อนมีบุตรจึงช่วยให้ครอบครัววางแผนได้ดีขึ้นและลดความเสี่ยงในการส่งต่อโรคนี้ไปยังรุ่นถัดไป แม้ปัจจุบันยังไม่มีวิธีรักษาให้หายขาด แต่การรักษาแบบควบคุมและดูแลอย่างใกล้ชิดสามารถช่วยให้ผู้ป่วยมีคุณภาพชีวิตที่ใกล้เคียงกับคนทั่วไปได้ มีการใช้ยาทำให้เลือดแข็งตัวมากขึ้นหรือฉีดโปรตีนช่วยเหลือเมื่อมีเลือดออก พร้อมทั้งหลีกเลี่ยงกิจกรรมเสี่ยงที่อาจทำให้เกิดบาดเจ็บ อีกประเด็นที่น่าสนใจคือ ความรู้และการรับรู้เกี่ยวกับโรคฮีโมฟีเลียยังไม่แพร่หลายมากนักในสังคม ซึ่งทำให้บางครอบครัวไม่รู้ตัวว่ามียีนผิดปกติในครอบครัวก่อนจะมีบุตร ดังนั้นการให้ความรู้ผ่านแพลตฟอร์มต่างๆ เป็นสิ่งสำคัญมากเพื่อให้ผู้คนตระหนักและเข้าถึงการตรวจคัดกรองได้ง่ายขึ้น โดยสรุป การทำความเข้าใจถึงลักษณะของโรคฮีโมฟีเลีย การรับรู้ว่าผู้หญิงสามารถเป็นพาหะได้ แม้ไม่มีอาการ และการตรวจคัดกรองก่อนการมีบุตร ถือเป็นกุญแจสำคัญในการป้องกันและจัดการโรคทางพันธุกรรมนี้อย่างมีประสิทธิภาพ สำหรับใครที่มีประวัติครอบครัวหรือมีความกังวล การปรึกษาแพทย์ผู้เชี่ยวชาญเป็นเรื่องที่ควรทำอย่างยิ่ง

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