
【医】 Abercrombie's degeneration
阿伯克龙比氏变性(Abercrombie’s degeneration)是淀粉样变性(amyloid degeneration)的旧称,指一种因淀粉样蛋白异常沉积在组织或器官中导致的病理改变。这类沉积可影响心脏、肾脏、肝脏、神经等多个系统,引发器官功能障碍,严重时危及生命。
建议进一步咨询专业医学文献或临床医生,以获取针对具体病例的诊断和治疗方案。
阿伯克龙比氏变性(ā bó kè lóng bǐ shì biàn xìng)是指一种罕见的遗传性疾病,又称为“5α-还原酶缺乏症”或“5α-还原酶缺陷症”。这种疾病会导致男性胚胎在子宫内发育时出现异常,最终导致患者在出生时或者在儿童时期出现男性外生殖器官不发育或者部分发育,出现女性化特征,如乳房发育和月经。
Abokelongbi syndrome (阿伯克龙比氏变性) is a rare genetic disease also known as "5α-reductase deficiency" or "5α-reductase defect". This disease can cause abnormal development of male embryos in the uterus, resulting in underdeveloped or partially developed male external genitalia at birth or in childhood, and the appearance of feminine characteristics such as breast development and menstruation.
Abokelongbi syndrome: /ˈæbəkɛlɒŋbi/
Abokelongbi syndrome is a medical condition that affects the development of male external genitalia in the womb. It is a rare genetic disease that can cause underdeveloped or partially developed male external genitalia, and result in the appearance of feminine characteristics.
Individuals with Abokelongbi syndrome may have ambiguous genitalia or be identified as female at birth, but develop a male gender identity later in life.(患有阿伯克龙比氏变性的人可能会出现不明显的生殖器官,或者在出生时被认为是女性,但后来发展出男性的性别认同。)
Abokelongbi syndrome is caused by a deficiency in the 5α-reductase enzyme, which is responsible for converting ************ into dihydro************ (DHT).(阿伯克龙比氏变性是由5α-还原酶缺乏引起的,该酶负责将睾丸激素转化为二氢睾丸激素(DHT)。)
5α-reductase deficiency(5α-还原酶缺乏症)
5α-reductase defect(5α-还原酶缺陷症)
There is no direct opposite term for Abokelongbi syndrome in English.
Abokelongbi syndrome is a medical term that is not commonly used in everyday conversation. it is an important term in the medical field for diagnosing and treating individuals with the condition.
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