WordNet
- make by small short touches that together produce an even or softly graded shadow, as in paint or ink
- produce a mottled effect; "The sunlight stippled the trees" (同)speckle
- apply (paint) in small dots or strokes
- engrave by means of dots and flicks
- the end of a long bone; initially separated from the main bone by a layer of cartilage that eventually ossifies so the parts become fused
PrepTutorEJDIC
- 〈U〉点彩(点画,点刻)[法] / 点彩(点画,点刻)による作品 / …‘を'点彩(点描,点刻)する
UpToDate Contents
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- 1. 致死的骨格形成異常の出生前診断 prenatal diagnosis of the lethal skeletal dysplasias
- 2. 大腿骨頭すべり症（SCFE）の評価およびマネージメント evaluation and management of slipped capital femoral epiphysis scfe
- 3. 小児における股関節痛の概要 overview of hip pain in childhood
- 4. 幼児、小児、および思春期における股関節の放射線学的評価 radiologic evaluation of the hip in infants children and adolescents
- 5. 小児における跛行の原因に関する概要 overview of the causes of limp in children
English Journal
- Maternal vitamin K deficient embryopathy: association with hyperemesis gravidarum and Crohn disease.
- Toriello HV1, Erick M, Alessandri JL, Bailey D, Brunetti-Pierri N, Cox H, Fryer A, Marty D, McCurdy C, Mulliken JB, Murphy H, Omlor J, Pauli RM, Ranells JD, Sanchez-Valle A, Tobiasz A, Van Maldergem L, Lin AE.
- American journal of medical genetics. Part A.Am J Med Genet A.2013 Mar;161A(3):417-29. doi: 10.1002/ajmg.a.35765. Epub 2013 Feb 12.
- Chondrodysplasia punctata (CDP) is an etiologically heterogeneous disorder characterized by the radiographic finding of stippled epiphyses (punctate calcifications). It is often accompanied by a characteristic facial appearance, known as the Binder phenotype, which is attributed to hypoplasia of the
- PMID 23404932
- Clinical and genetic analysis of a Korean patient with X-linked chondrodysplasia punctata: identification of a novel splicing mutation in the ARSE gene.
- Jeon GW1, Kwon MJ, Lee SJ, Sin JB, Ki CS.
- Annals of clinical and laboratory science.Ann Clin Lab Sci.2013 Winter;43(1):70-5.
- X-linked recessive chondrodysplasia punctata (CDPX1) is a rare congenital disorder of bone and cartilage development, characterized by punctate calcification in areas of endochondral bone formation, leading to stippled epiphyses, severe nasal and midfacial hypoplasia, short stature, and brachyteleph
- PMID 23462608
- Metaphyseal chondromatosis combined with D-2-hydroxyglutaric aciduria in four patients.
- Choo HJ1, Cho TJ, Song J, Tiller GE, Lee SH, Park G, Lee IS, Lachman R, Superti-Furga A, Kim OH.
- Skeletal radiology.Skeletal Radiol.2012 Nov;41(11):1479-87. Epub 2012 May 26.
- We report four patients who presented with a severe form of metaphyseal chondromatosis in association with D-2-hydroxyglutaric aciduria (D-2-HGA). All patients showed splaying columns of irregular ossification defects with bulbous metaphyses of the long tubular bones, as well as remarkable involveme
- PMID 22639207
Related Links
- stip·pled epiphysis (st p ld) n. A congenital abnormality of the epiphyses marked by multiple ossification centers that severely deform the long bone and give it a stippled appearance and a thickened shaft. Also called dysplasia ...
- Medical Dictionary stippled epiphysis stip·pled epiphysis (stĭp'əld) n. A congenital abnormality of the epiphyses marked by multiple ossification centers that severely deform the long bone and give it a stippled appearance and a ...
Related Pictures
★リンクテーブル★
| リンク元 | 「斑点状骨端症」 |
| 関連記事 | 「stipple」 |
「斑点状骨端症」
「stipple」
- n.
- 点描/点彩/点刻(法)
- vt.vi.
- 点描/点彩/点刻する。～に反転をつける。
- lead poisoning would produce microcytosis with basophilic stippling.