異形成、形成不全、形成異常、形成不全症、形成異常症、発育異常、異発生
- 関
- aplasia、aplastic、dysgenetic、dysgenic、dysplasia、dysplastic、heteroplasia、heteroplasmy、hypoplasia、malformation、metaplasia、metaplastic
WordNet
- infertility between hybrids
- relating to or evidencing dysplasia
- abnormal development (of organs or cells) or an abnormal structure resulting from such growth
- something abnormal or anomalous (同)miscreation
- pertaining to or causing degeneration in the offspring produced (同)cacogenic
- underdevelopment of an organ because of a decrease in the number of cells
PrepTutorEJDIC
- (特に生物体の)奇形;{C}奇形部分
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2015/07/13 00:19:20」(JST)
wiki en
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.
- 1. 先天性腎尿路異常（CAKUT）の概要 overview of congenital anomalies of the kidney and urinary tract cakut
- 2. Renal hypodysplasia
- 3. 重度複合型免疫不全（SCID）：特定の欠損 severe combined immunodeficiency scid specific defects
- 4. 先天性甲状腺機能低下症の臨床的特徴および検出 clinical features and detection of congenital hypothyroidism
- 5. Testicular germ cell neoplasia in situ (formerly called intratubular germ cell neoplasia of unclassified type)
English Journal
- Dysmorphologic assessment in 115 Mayer-Rokitansky-Küster-Hauser patients.
- Lalatta F1, Motta F, Restelli E, Bellini M, Miozzo M, Gervasini C, Dallapiccola B, Gentilin B, Fedele L.
- Clinical dysmorphology.Clin Dysmorphol.2015 Jul;24(3):95-101. doi: 10.1097/MCD.0000000000000087.
- Mayer-Rokitansky-Küster-Hauser (MRKH) patients are characterized by congenital aplasia of the uterus and the upper part of the vagina, with normal secondary sexual characteristics. This disorders affects one in 4000-5000 females and it is classified as typical, type I or isolated, and as atypical,
- PMID 25968587
- Congenital Thoracic Venous Anomalies in Adults: Morphologic MR Imaging.
- Ruano CA1, Marinho-da-Silva A2, Donato P3.
- Current problems in diagnostic radiology.Curr Probl Diagn Radiol.2015 Jul-Aug;44(4):337-345. doi: 10.1067/j.cpradiol.2015.01.002. Epub 2015 Jan 24.
- Congenital anomalies of the thoracic veins are rare yet important developmental abnormalities, usually classified into systemic and pulmonary. They may be encountered incidentally; as such the radiologist must be aware of their imaging presentation and clinical relevance. Furthermore, to understand
- PMID 25953438
- Safety of octreotide in hospitalized infants.
- Testoni D1, Hornik CP2, Neely ML3, Yang Q4, McMahon AW5, Clark RH6, Smith PB7; Best Pharmaceuticals for Children Act — Pediatric Trials Network Administrative Core Committee.
- Early human development.Early Hum Dev.2015 Jul;91(7):387-92. doi: 10.1016/j.earlhumdev.2015.04.008. Epub 2015 May 15.
- BACKGROUND: Octreotide is used off-label in infants for treatment of chylothorax, congenital hyperinsulinism, and gastrointestinal bleeding. The safety profile of octreotide in hospitalized infants has not been described; we sought to fill this information gap.METHODS: We identified all infants expo
- PMID 25968047
- Potocki-Lupski syndrome in conjunction with bilateral clubfoot.
- Dhanaraj D1, Chu A, Pappas JG, Moran E, Lehman WB.
- Journal of pediatric orthopedics. Part B.J Pediatr Orthop B.2015 Jul;24(4):373-6. doi: 10.1097/BPB.0000000000000131.
- Potocki-Lupski syndrome (PTLS) is a rare chromosomal microduplication syndrome resulting in multiple congenital abnormalities including developmental delays, autistic features, and certain structural anomalies, with cardiovascular being the most common. The phenotype of this contiguous gene duplicat
- PMID 25768679
Japanese Journal
- 甲状腺疾患にかかわる遺伝子異常 (特集 甲状腺疾患 : 診断・治療の最新動向) -- (病因および疾患関連遺伝子)
- 菱沼 昭
- 日本臨床 70(11), 1885-1891, 2012-11
- NAID 40019466265
- 高度な精巣微小石灰化を伴う非閉塞性無精子症に対しMicrodissection TESE を施行し精子を採取し得た1例
- 竹澤 健太郎,金城 孝則,種田 建史 [他]
- 泌尿器科紀要 = Acta urologica Japonica 58(10), 575-577, 2012-10
- … Testicular microlithiasis has been reported to be an infrequent condition associated with conditions such as testicular tumors and testicular dysgenesis syndrome. …
- NAID 40019492270
- 前眼部の形態変化を観察できた前眼部形成不全の1例
- 國原 依里子,竹中 丈二,近間 泰一郎,木内 良明
- 日本眼科學会雜誌 116(7), 650-656, 2012-07-10
- NAID 10030791171
Related Links
- Dysgenesis may refer to: Dysgenesis (embryology), which indicates abnormal organ development during embryonic growth and development; Anterior segment dysgenesis, a failure of the normal development of the tissues of the anterior ...
- Gonadal dysgenesis is a term used to describe multiple reproductive system development disorders. They are conditions of genetic origin. It is characterized by a progressive loss of primordial germ cells on the developing gonads of an ...
Related Pictures
★リンクテーブル★
| リンク元 | 「発育異常」「形成不全」「dysgenic」「形成異常」「異発生」 |
| 拡張検索 | 「46,XY gonadal dysgenesis」「45,X gonadal dysgenesis」「46,XX gonadal dysgenesis」「complete gonadal dysgenesis」 |
「発育異常」
- 英
- developmental anomalies, dysgenesis、dysgenic
- ラ
- dysontogenia
- 同
- 成長異常 abnormal growth
- 関
- 異形成、異発生、逆選択、形成異常、形成不全、ディスジェニック、形成異常症、形成不全症
「形成不全」
「dysgenic」
- 発育異常の、異形成の、逆選択の、異発生の
- 関
- adverse selection、dysgenesis、dysgenetic、dysplasia、heteroplasia、heteroplasmy、metaplasia、metaplastic
「形成異常」
「異発生」
「46,XY gonadal dysgenesis」
「45,X gonadal dysgenesis」
45
「46,XX gonadal dysgenesis」
46、XX型性腺形成異常症