| 词条 | Sclerocornea |
| 释义 |
| name = Sclerocornea | synonyms = | image = Autosomal dominant - en.svg | image_size = 150px | caption = This condition can be inherited in an autosomal dominant manner | pronounce = | field = | symptoms = | complications = | onset = | duration = | types = | causes = | risks = | diagnosis = | differential = | prevention = | treatment = | medication = | prognosis = | frequency = | deaths = }} Sclerocornea is a congenital anomaly of the eye in which the cornea blends with sclera, having no clear-cut boundary. The extent of the resulting opacity varies from peripheral to total (sclerocornea totalis). The severe form is thought to be inherited in an autosomal recessive manner, but there may be another, milder form that is expressed in a dominant fashion. In some cases the patients also have abnormalities beyond the eye (systemic), such as limb deformities and craniofacial and genitourinary defects. According to one tissue analysis performed after corneal transplantation, the sulfation pattern of keratan sulfate proteoglycans in the affected area is typical for corneal rather than scleral tissue.[1] Sclerocornea may be concurrent with cornea plana. {{clear}}References1. ^{{cite journal |vauthors=Young RD, Quantock AJ, Sotozono C, Koizumi N, Kinoshita S |title=Sulphation patterns of keratan sulphate proteoglycan in sclerocornea resemble cornea rather than sclera |journal=Br J Ophthalmol |volume=90 |issue=3 |pages=391–3 |date=March 2006 |pmid=16488970 |pmc=1856931 |doi=10.1136/bjo.2005.085803 |url=http://bjo.bmj.com/cgi/pmidlookup?view=long&pmid=16488970}} External links{{Medical resources| DiseasesDB = | ICD10 = Q13.3 | ICD9 = | ICDO = | OMIM = 269400 | OMIM_mult = {{OMIM2|181700}} | MedlinePlus = | eMedicineSubj = | eMedicineTopic = | MeshID = | Orphanet = 91490 }}
1 : Diseases of the eye and adnexa |
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