| 词条 | Rosenthal–Kloepfer syndrome |
| 释义 |
| name = | synonym = Familial pachydermoperiostosis | image = | image_size = | alt = | caption = | pronounce = | specialty = | symptoms = | complications = | onset = | duration = | types = | causes = | risks = | diagnosis = | differential = | prevention = | treatment = | medication = | prognosis = | frequency = | deaths = }} Rosenthal–Kloepfer syndrome, is a cutaneous condition characterized by abnormal growth of bone and skin, coupled with clouding of the cornea.[1] It was described in 1962.[2] Another name for the condition is Acromegaly-cutis verticis gyrata-corneal leukoma syndrome. Signs and SymptomsPresenting symptoms include unilateral or bilateral opacification of the cornea, which progressively involves the whole structure. Visual disturbance secondary to corneal opacification is often the presenting symptom. Other symptoms include furrowing of the scalp, enlargement of the bony portion of the eyebrows, and disproportionately large hands.[3] CauseNo gene mutation as has been associated with this disorder. Inheritance follows an autosomal dominant pattern. DiagnosisRadiographic imaging reveals thickening of bones, especially of the skull, and widening of the bones in the fingers.[4]See also
References1. ^{{Cite web|url=http://disorders.eyes.arizona.edu/handouts/rosenthal-kloepfer-syndrome|title=Rosenthal-Kloepfer Syndrome {{!}} Hereditary Ocular Diseases|website=disorders.eyes.arizona.edu|language=en|access-date=2018-02-27}} 2. ^{{cite journal |vauthors=ROSENTHAL JW, KLOEPFER HW |title=An acromegaloid, cutis verticis gyrata, corneal leukoma syndrome. A new medical entity |journal=Arch. Ophthalmol. |volume=68 |issue= |pages=722–6 |date=December 1962 |pmid=13974983 |doi=10.1001/archopht.1962.00960030726004 |url=http://archopht.ama-assn.org/cgi/pmidlookup?view=long&pmid=13974983 |archive-url=https://archive.is/20120306080035/http://archopht.ama-assn.org/cgi/pmidlookup?view=long&pmid=13974983 |dead-url=yes |archive-date=2012-03-06 }} 3. ^{{Cite web|url=http://disorders.eyes.arizona.edu/handouts/rosenthal-kloepfer-syndrome|title=Rosenthal-Kloepfer Syndrome {{!}} Hereditary Ocular Diseases|website=disorders.eyes.arizona.edu|language=en|access-date=2018-02-27}} 4. ^{{Cite web|url=http://disorders.eyes.arizona.edu/handouts/rosenthal-kloepfer-syndrome|title=Rosenthal-Kloepfer Syndrome {{!}} Hereditary Ocular Diseases|website=disorders.eyes.arizona.edu|language=en|access-date=2018-02-27}} External links{{Medical resources| DiseasesDB = | ICD10 = | ICD9 = | ICDO = | OMIM = 102100 | MedlinePlus = | eMedicineSubj = | eMedicineTopic = | MeshID = | GeneReviewsName = | Orphanet = 964 }}{{DEFAULTSORT:Rosenthal-Kloepfer syndrome}}{{Dermatology-stub}} 3 : Cutaneous congenital anomalies|Genetic disorders with OMIM but no gene|Syndromes |
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