無毛症、無毛
- 関
- atrichous、glabrous、hairless
WordNet
- having no hair or fur; "a Mexican Hairless is about the size of a fox terrier and hairless except for a tufts on the head and tail"
- having no hair or similar growth; smooth; "glabrous stems"; "glabrous leaves"; "a glabrous scalp"
PrepTutorEJDIC
- 髪のない,はげの
- (動植物が)無毛の
UpToDate Contents
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English Journal
- Microcephaly, ectodermal dysplasia, multiple skeletal anomalies and distinctive facial appearance: delineation of cerebro-dermato-osseous-dysplasia.
- Castori M1, Pascolini G, Parisi V, Sana ME, Novelli A, Nürnberg P, Iascone M, Grammatico P.
- American journal of medical genetics. Part A.Am J Med Genet A.2015 Apr;167A(4):842-51. doi: 10.1002/ajmg.a.36983. Epub 2015 Feb 23.
- In 1980, a novel multiple malformation syndrome has been described in a 17-year-old woman with micro- and turricephaly, intellectual disability, distinctive facial appearance, congenital atrichia, and multiple skeletal anomalies mainly affecting the limbs. Four further sporadic patients and a couple
- PMID 25708316
- Trichoscopic findings of androgenetic alopecia and their association with disease severity.
- Hu R1, Xu F, Han Y, Sheng Y, Qi S, Miao Y, Yang Q.
- The Journal of dermatology.J Dermatol.2015 Mar 26. doi: 10.1111/1346-8138.12857. [Epub ahead of print]
- Trichoscopy is a novel tool for the diagnosis of hair loss disorders such as androgenetic alopecia (AGA), but there are still few reports on the association between trichoscopic findings and disease severity, especially in the Chinese population. A case-control observational study was conducted to o
- PMID 25810236
- Ichthyosis follicularis, atrichia, and photophobia syndrome associated with a new mutation in MBTPS2.
- Fong K1, Takeichi T, Liu L, Pramanik R, Lee J, Akiyama M, McGrath JA.
- Clinical and experimental dermatology.Clin Exp Dermatol.2015 Feb 16. doi: 10.1111/ced.12587. [Epub ahead of print]
- Ichthyosis follicularis, atrichia and photophobia (IFAP) syndrome (OMIM 308205) is a rare X-linked genetic disorder. Mutations in MBTPS2 underlie IFAP syndrome, with 19 different mutations reported to date. Keratosis follicularis spinulosa decalvans (KFSD) is an allelic disorder that results from a
- PMID 25683132
Japanese Journal
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- AZEEM Zahid,WASIF Naveed,BASIT Sulman,RAZAK Suhail,AMJAD WAHEED Raja,ISLAM Adeel,AYUB Muhammad,KAFAITULLAH,KAMRAN-UL-HASSAN NAQVI Syed,ALI Ghazanfar,AHMAD Wasim
- Journal of dermatology 38(8), 755-760, 2011-08-01
- NAID 10031147083
- A Japanese case of ichthyosis follicularis with atrichia and photophobia syndrome with an MBTPS2 mutation
- Nakayama Junko,Iwasaki Nobuaki,Shin Kenji [他],SATO Hideo,KAMO Mariko,OHYAMA Manabu,NOGUCHI Emiko,ARINAMI Tadao
- Journal of human genetics 56(3), 250-252, 2011-03-01
- NAID 10030658580
- Mutations in the hairless gene underlie APL in three families of Pakistani origin
- KRAEMER Liv,WAJID Muhammad,SHIMOMURA Yutaka,CHRISTIANO Angela M.
- Journal of dermatological science 50(1), 25-30, 2008-04-01
- NAID 10031136033
Related Links
- Wikipedia encyclopedia ? atrichia. Also found in: Dictionary/thesaurus, Encyclopedia, 0.01 sec. a·trich·i·a ( -tr k - , -tr k -). n. The congenital or acquired absence of hair. Also called atrichosis. atrichia. [ātrik′ē·ə]. Etymology: Gk, a, not, thrix, hair ...
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- 英
- atrichia、hairless、glabrous、atrichous
- 関
- 無毛症、無毛性
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- atrichia、glabrous、hairless
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- atrichia、atrichous、hairless
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- atrichia、atrichous、glabrous
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