
【医】 cystine diathesis
【机】 ar-
model; pattern
twin; two
【计】 binary-coded decimal; binary-coded decimal character code
binary-to-decimal conversion; binary-to-hexadecimal conversion
【医】 bi-; bis-; di-; duo-
family name; surname
【医】 complex; symptom complex; symptom grouping; symptom-complex
symptom-group; symptomes complice; syndrome
阿-范二氏综合征(Cystine Diathesis)是一种罕见的遗传性代谢疾病,主要与胱氨酸代谢异常相关。以下是详细解释:
由于该信息源自低权威性网页,建议通过权威医学数据库(如UpToDate、PubMed)或咨询遗传代谢科医生进一步核实。若出现相关症状,请及时就医。
阿-范二氏综合征(Aarskog-Scott syndrome),又称作“面部骨骼畸形-生殖发育不良综合征”、“矮小面容综合征”、“手脚短小面容特征综合征”等,是一种罕见的遗传性疾病,主要表现为身材矮小、面容特征不明显,手脚短小,肢体发育不良,和生殖系统的异常发育。
Ā-fàn-èr-shì zòng-hé zhèng
Aarskog-Scott syndrome, also known as "facial bone malformation-genital development disorder syndrome", "short stature facial feature syndrome", "short hands and feet facial feature syndrome", etc., is a rare genetic disease that mainly manifests as short stature, indistinct facial features, small hands and feet, limb malformation, and abnormal development of the reproductive system.
/ɑrskɔg skɔt sɪndrom/
The Aarskog-Scott syndrome is a rare genetic disease that affects the growth and development of individuals.
The Aarskog-Scott syndrome is characterized by short stature, facial abnormalities, and genital anomalies.(阿-范二氏综合征的特点是身材矮小、面部畸形和生殖器异常。)
The Aarskog-Scott syndrome is inherited in an X-linked pattern.(阿-范二氏综合征以X染色体显性遗传为主。)
Aarskog-Scott syndrome is a medical term that is not commonly used in everyday language.
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