遺伝性象牙質形成不全症
WordNet
- an appreciable consequence (especially a lessening); "it made a dent in my bank account"
- an impression in a surface (as made by a blow) (同)ding, gouge, nick
- underdevelopment of an organ because of a decrease in the number of cells
PrepTutorEJDIC
- くぼみ,へこみ / …‘を'くぼませる,へこませる / へこむ,くぼむ
- (くし・歯車などの)歯
- 世襲の,親譲りの / 遺伝的な,遺伝性の
UpToDate Contents
全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.
English Journal
- Multiple teeth fractures in dentinogenesis imperfecta: a case report.
- Min B1, Song JS, Lee JH, Choi BJ, Kim KM, Kim SO.
- The Journal of clinical pediatric dentistry.J Clin Pediatr Dent.2014 Summer;38(4):362-5.
- Dentinogenesis imperfecta (DGI) is a hereditary defect consisting of opalescent teeth composed of irregularly formed and hypomineralized dentin. This paper presents the multiple fractures of DGI-affected teeth and suggests the reason of low fracture resistance by observing the dentin microstructures
- PMID 25571690
- An overview of molecular and genetic alterations in selected benign odontogenic disorders.
- Cabay RJ1.
- Archives of pathology & laboratory medicine.Arch Pathol Lab Med.2014 Jun;138(6):754-8. doi: 10.5858/arpa.2013-0057-SA.
- CONTEXT: Some dental abnormalities have environmental causes. Other odontogenic alterations are idiopathic and may have hereditary etiologies. Investigations of these conditions are ongoing.OBJECTIVE: To provide a discussion of developmental odontogenic abnormalities and benign odontogenic overgrowt
- PMID 24878015
- Oral and craniofacial manifestations and two novel missense mutations of the NTRK1 gene identified in the patient with congenital insensitivity to pain with anhidrosis.
- Gao L1, Guo H, Ye N, Bai Y, Liu X, Yu P, Xue Y, Ma S, Wei K, Jin Y, Wen L, Xuan K.
- PloS one.PLoS One.2013 Jun 14;8(6):e66863. doi: 10.1371/journal.pone.0066863. Print 2013.
- Congenital insensitivity to pain with anhidrosis (CIPA) is a rare inherited disorder of the peripheral nervous system resulting from mutations in neurotrophic tyrosine kinase receptor 1 gene (NTRK1), which encodes the high-affinity nerve growth factor receptor TRKA. Here, we investigated the oral an
- PMID 23799134
Japanese Journal
- 自然発症肝炎・肝癌ラット(LECラット)における着色歯の検索 第1報 病理組織学的検討:第1報: 病理組織学的検討
- 渡辺 一史,柴田 敏之,加藤 元康,永易 裕樹,大森 一幸,窪田 正樹,有末 眞,村瀬 博文
- 日本口腔科学会雑誌 42(2), 243-250, 1993
- … We noticed that the green-pigmented incisors in LEC rat erupted 3 weeks after hereditary acute hepatitis. … The green pigmentation was observed as a green stripe in the dentin and the stripe ran parallel to the incremental line. … These results suggested that acute hepatitis and jaundice in LEC rat caused green-pigmented incisors and hypocalcification and hypoplasia of the matrix in the dentin, and we suspected that pigmentation was caused by bilirubin. …
- NAID 130004335386
Related Links
- Hereditary Hypoplasia of the Dentin * George W. Wilson, D.D.S., F.A.C.D., Matilda Steinbrecher, B.Sc. Milwaukee, Wis. Available online 13 January 2015 Show more Show less Choose an option to locate/access this article: ...
- 1.Attrition 2.Abrasion 3.Erosion 4.Abfraction lesions 5.Localized non-hereditary Enamel Hypoplasia 6.Localized non-hereditary Enamel Hypocalcification 7.Localized non-hereditary Dentin Hypoplasia 8.Localized non-hereditary Dentin ...
★リンクテーブル★
[★]
- 英
- hereditary dentin hypoplasia
- ラ
- dentinogenesis imperfecta
- 同
- 遺伝性乳白色象牙質 hereditary opalescent dentin、カプドポン病 Capdepont disease
[★]
- 関
- abortion、abortive、agenesis、、dysgenesis、hypotrophy
- 無形成、aplasia、aplastic
[★]
- 関
- heredity、heritable、inherit、inheritable、inheritable character、inheritance、inherited
[★]
- 関
- dental、dentistry