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- This disorder is inherited as an autosomal dominant trait. 本病作為常染色體顯性傳遞。
- Tuberous sclerosis (TSC) is a common autosomal dominant disease. 結節性硬化癥是一種臨床較常見(jiàn)的顯性遺傳病。
- HHT is an autosomal dominant disordercharacterized by vascular dysplasia. HHT是常染色體顯性遺傳性血管發(fā)育異常的一種疾病。
- It is obviously autosomal dominant inheritance according to the pedigree. 由于第一代病例僅為右眼虹膜缺損，故較支持中胚層迷走發(fā)育的理論。
- The Alzheimer in this ancestry appears as autosomal dominant genetic disease. 阿爾茨海默病在本家系中顯示為常染色體顯性遺傳。
- With pedigree analysis, the genetic mode of the disease in the family are autosomal dominant inheritance. 據系譜分析,該疾病符合常染色體顯性遺傳方式。
- A Six-generation Family with Autosomal Dominant Deafness Passed Along: Possibly A New Locus? 六代相傳顯性遺傳耳聾大家系:一個(gè)可能的新基因座?
- Objective: To study the effects of rhodopsin (RHO) gene in autosomal dominant retinitis pigmentosa (adRP). 摘要目的：探討視紫紅質(zhì)基因在視網(wǎng)膜色素變性疾病中的作用。
- Neurofibromatosis is an autosomal dominant genetic disease, which also named as Von Recklinghausen disease before. 神經(jīng)纖維瘤病，以前又稱(chēng)von Recknn沙ausen病，屬常染色體顯性遺傳病。
- Dentinogenesis imperfecta (DI) is a kind of mesodermal defect inherited in a simple autosomal dominant mode. 摘要牙本質(zhì)形成不良是一種體染色體顯性遺傳的中胚層缺陷。
- Peutz-Jeghers, also known as Hereditary Intestinal Polyposis Syndrome, is an autosomal dominant genetic disease. 什么是'黑斑息肉綜合征-多生長(cháng)在腸道'?
- Objective To analyze the occurrence character of autosomal dominant familial polycystic kidney. 目的分析常染色體顯性遺傳多囊腎的發(fā)病特點(diǎn)。
- According to genetic analysis, this disease is caused by autosomal dominant inheritance. 經(jīng)過(guò)遺傳分析，認為該畸形屬常染色體顯性遺傳。
- Conclusion The congenital teeth agenesis maily is autosomal dominant inheritant disease. 結論先天缺牙家系多為常染色體顯性遺傳；
- It can be autosomal dominant, autosomal recessive, or X-linked mode of inheritance. 他可以是體染色體顯性、體染色體隱性、或是性聯(lián)遺傳等方式的遺傳疾病。
- Dentin dysplasia is a genetic disorder of teeth, commonly exhibiting an autosomal dominant inheritance. 什麼是'牙本質(zhì)發(fā)育異常-牙本質(zhì)發(fā)育異常'?
- Some members of the patient s family were similarly affected and indicated an autosomal dominant trait of inheritance. 一些親屬亦有類(lèi)似病癥，顯示是體顯性遺傳模式。
- Objective A case of Autosomal dominant pigmentary type of orthochromatic leukodstrophy(POLD) was reported. 目的探討顯性遺傳性色素顆粒型正染性腦白質(zhì)營(yíng)養不良的臨床和病理改變特點(diǎn)。
- As with familial adenomatous polyposis, the inheritance pattern is autosomal dominant. 家族性腺瘤息肉病的遺傳方式是常染色體顯性遺傳。
- Conclusion:EXT is an autosomal dominant disorder and the penetrance is 97%in this report. 結論：證實(shí)EXT為常染色體顯性遺傳病，本組外顯率為97%25。
