congenital afibrinogenemia
Simplified Chinese_translation
hereditary afibrinogenemia
Simplified Chinese_translation
severe afibrinogenemia
Simplified Chinese_translation
afibrinogenemia treatment
Simplified Chinese_translation
afibrinogenemia diagnosis
Simplified Chinese_translation
diagnosing afibrinogenemia
Simplified Chinese_translation
afibrinogenemia symptoms
Simplified Chinese_translation
treating afibrinogenemia
Simplified Chinese_translation
afibrinogenemia testing
Simplified Chinese_translation
acquired afibrinogenemia
Simplified Chinese_translation
congenital afibrinogenemia is a rare bleeding disorder characterized by the complete absence of fibrinogen in the blood.
先天性无纤维蛋白原血症是一种罕见的出血性疾病,其特点是血液中完全缺乏纤维蛋白原。
patients with afibrinogenemia experience prolonged bleeding from minor wounds and spontaneous bruising.
无纤维蛋白原血症患者会因轻微伤口出现长时间出血,并伴有自发性瘀伤。
the diagnosis of afibrinogenemia requires specialized blood tests to confirm the absence of fibrinogen.
无纤维蛋白原血症的诊断需要进行专门的血液检测以确认纤维蛋白原的缺失。
afibrinogenemia treatment typically involves replacement therapy with fibrinogen concentrate.
无纤维蛋白原血症的治疗通常涉及使用纤维蛋白原浓缩物进行替代治疗。
inherited afibrinogenemia follows an autosomal recessive pattern of inheritance.
遗传性无纤维蛋白原血症遵循常染色体隐性遗传模式。
medical research on afibrinogenemia has led to improved treatment protocols in recent years.
近年来对无纤维蛋白原血症的医学研究已导致治疗方案的改善。
severe afibrinogenemia can cause life-threatening internal bleeding complications.
严重的无纤维蛋白原血症可能导致危及生命的内出血并发症。
genetic counseling is essential for families affected by afibrinogenemia.
对于受无纤维蛋白原血症影响的家庭,遗传咨询是必不可少的。
newborn screening can help detect afibrinogenemia early in infants.
新生儿筛查有助于早期发现婴儿的无纤维蛋白原血症。
afibrinogenemia management requires a comprehensive approach including preventive care.
无纤维蛋白原血症的管理需要包括预防性护理在内的综合方法。
the prognosis for afibrinogenemia has improved significantly with modern treatments.
随着现代治疗方法的出现,无纤维蛋白原血症的预后已显著改善。
scientists continue to study the genetic mutations responsible for afibrinogenemia.
科学家们继续研究导致无纤维蛋白原血症的遗传突变。
congenital afibrinogenemia
Simplified Chinese_translation
hereditary afibrinogenemia
Simplified Chinese_translation
severe afibrinogenemia
Simplified Chinese_translation
afibrinogenemia treatment
Simplified Chinese_translation
afibrinogenemia diagnosis
Simplified Chinese_translation
diagnosing afibrinogenemia
Simplified Chinese_translation
afibrinogenemia symptoms
Simplified Chinese_translation
treating afibrinogenemia
Simplified Chinese_translation
afibrinogenemia testing
Simplified Chinese_translation
acquired afibrinogenemia
Simplified Chinese_translation
congenital afibrinogenemia is a rare bleeding disorder characterized by the complete absence of fibrinogen in the blood.
先天性无纤维蛋白原血症是一种罕见的出血性疾病,其特点是血液中完全缺乏纤维蛋白原。
patients with afibrinogenemia experience prolonged bleeding from minor wounds and spontaneous bruising.
无纤维蛋白原血症患者会因轻微伤口出现长时间出血,并伴有自发性瘀伤。
the diagnosis of afibrinogenemia requires specialized blood tests to confirm the absence of fibrinogen.
无纤维蛋白原血症的诊断需要进行专门的血液检测以确认纤维蛋白原的缺失。
afibrinogenemia treatment typically involves replacement therapy with fibrinogen concentrate.
无纤维蛋白原血症的治疗通常涉及使用纤维蛋白原浓缩物进行替代治疗。
inherited afibrinogenemia follows an autosomal recessive pattern of inheritance.
遗传性无纤维蛋白原血症遵循常染色体隐性遗传模式。
medical research on afibrinogenemia has led to improved treatment protocols in recent years.
近年来对无纤维蛋白原血症的医学研究已导致治疗方案的改善。
severe afibrinogenemia can cause life-threatening internal bleeding complications.
严重的无纤维蛋白原血症可能导致危及生命的内出血并发症。
genetic counseling is essential for families affected by afibrinogenemia.
对于受无纤维蛋白原血症影响的家庭,遗传咨询是必不可少的。
newborn screening can help detect afibrinogenemia early in infants.
新生儿筛查有助于早期发现婴儿的无纤维蛋白原血症。
afibrinogenemia management requires a comprehensive approach including preventive care.
无纤维蛋白原血症的管理需要包括预防性护理在内的综合方法。
the prognosis for afibrinogenemia has improved significantly with modern treatments.
随着现代治疗方法的出现,无纤维蛋白原血症的预后已显著改善。
scientists continue to study the genetic mutations responsible for afibrinogenemia.
科学家们继续研究导致无纤维蛋白原血症的遗传突变。
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