色素変性
WordNet
- the process of declining from a higher to a lower level of effective power or vitality or essential quality (同)devolution
- passing from a more complex to a simpler biological form (同)retrogression
PrepTutorEJDIC
- 退歩,退化,墜落
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
- Acquired Bilateral Dyspigmentation on Face and Neck: Clinically Appropriate Approaches.
- Lee YJ1, Park JH1, Lee DY1, Lee JH1,2.
- Journal of Korean medical science.J Korean Med Sci.2016 Dec;31(12):2042-2050. doi: 10.3346/jkms.2016.31.12.2042.
- Facial dyspigmentation in Asian women often poses diagnostic and therapeutic challenges. Recently, a distinctive bilateral hyperpigmentation of face and neck has occasionally been observed. This study was performed to investigate the clinico-pathological features of this dyspigmentation as well as p
- PMID 27822947
- Spectrum of ocular manifestations in cobalamin C and cobalamin A types of methylmalonic acidemia.
- Ku CA1, Ng JK1, Karr DJ1, Reznick L1, Harding CO2, Weleber RG1, Pennesi ME1.
- Ophthalmic genetics.Ophthalmic Genet.2016 Dec;37(4):404-414. Epub 2016 Mar 15.
- BACKGROUND: Cobalamin C disease (cblC), which leads to methylmalonic acidemia with homocystinuria, is the most common inherited disorder of vitamin B12 metabolism. Reported ocular findings associated with cblC have been maculopathy, pigmentary retinopathy, and optic nerve atrophy. Cobalamin A diseas
- PMID 26979128
- Mislocalisation of BEST1 in iPSC-derived retinal pigment epithelial cells from a family with autosomal dominant vitreoretinochoroidopathy (ADVIRC).
- Carter DA1, Smart MJ1, Letton WV1, Ramsden CM1,2, Nommiste B1, Chen LL1, Fynes K1, Muthiah MN2, Goh P3, Lane A1, Powner MB1, Webster AR1,2, da Cruz L1,2, Moore AT1,2,4, Coffey PJ1, Carr AF1.
- Scientific reports.Sci Rep.2016 Sep 22;6:33792. doi: 10.1038/srep33792.
- Autosomal dominant vitreoretinochoroidopathy (ADVIRC) is a rare, early-onset retinal dystrophy characterised by distinct bands of circumferential pigmentary degeneration in the peripheral retina and developmental eye defects. ADVIRC is caused by mutations in the Bestrophin1 (BEST1) gene, which encod
- PMID 27653836
Japanese Journal
- 網膜色素変性の長期予後 : 情報提供のあり方を考える
- 岩田 文乃
- 眼科臨床紀要 = Folia Japonica de ophthalmologica clinica 1(11), 1108, 2008-11-15
- NAID 10023922290
- 第12回徳島医学会賞受賞論文 バイアグラ(一般名:クエン酸シルデナフィル)の使用経験と前後研究による効果評価(1)来院者の特徴
- 小倉 邦博,Ogura Kunihiro
- 四国医学雑誌 60(3・4), 80-86, 2004-08-25
- … Pigmentary retinal degeneration（PRD）is classifiedas one of Sildenafil's contraindications. …
- NAID 120004631547
- 白内障手術を施行した網膜色素変性症患者の Quality of Life (QOL)
- 江口 万祐子,中村 昌弘,林 振民,筑田 眞
- IOL & RS : Japanese journal of cataract and refractive surgery : 日本眼内レンズ屈折手術学会誌 18(2), 151-156, 2004-06-01
- NAID 10013798510
Related Links
- This is a rare syndrome consisting of a pigmentary degeneration of the retina in association with nanophthalmos. The globe is small with a thickened choroid and sclera and the macula becomes atrophic later in life. Some patients ...
- Definition of primary pigmentary degeneration of retina in the Medical Dictionary. primary pigmentary degeneration of retina explanation. Information about primary pigmentary degeneration of retina in Free online English dictionary ...
★リンクテーブル★
[★]
- 英
- pigmentation, chromatosis
- 同
- 色素変性 pigmentary degeneration
[★]
- 英
- pigmentary degeneration
- 関
- 色素沈着
[★]
淡蒼球色素変性症。ハラーフォルデン・シュパッツ病
[★]
- 関
- degeneracy、degenerate、degenerative、denaturation、denature、involution、retract、retrograde degeneration、retrograde degradation、unfolding
[★]
- 関
- pigmented