hereditary progressive arthro-ophthalmopathy

hereditary progressive arthro-ophthalmopathy
an autosomal dominant disorder consisting of myopia progressing to retinal detachment and blindness, and premature degenerative changes in the joints; sensorineural deafness may also occur. Called also Stickler syndrome.

Medical dictionary. 2011.

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Look at other dictionaries:

  • Stickler syndrome — Infobox Disease Name = Stickler syndrome Caption = DiseasesDB = 29327 ICD10 = ICD10|Q|87|8|q|80 ICD9 = ICD9|756.0 ICDO = OMIM = 108300 OMIM mult = OMIM2|277610 OMIM2|184840 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Stickler syndrome …   Wikipedia

  • artrooftalmopatía hereditaria progresiva — Eng. Hereditary progressive arthro ophthalmopathy Ver síndrome de Stickler …   Diccionario de oftalmología

  • síndrome de artrooftalmopatía progresiva hereditaria — Eng. Hereditary progressive arthro ophthalmopathy syndrome Ver síndrome de Stickler …   Diccionario de oftalmología

  • Stickler syndrome — Stick·ler syndrome stik lər n a variable disorder of connective tissue involving the skeleton, face, and eyes that is characterized by myopia, retinal detachment, cleft palate, micrognathia, flat facies, premature arthritis, hip deformity, and… …   Medical dictionary

  • Marshall syndrome — a rare, autosomal dominant syndrome characterized by ectodermal dysplasia, hypertelorism, myopia progressing to retinal detachment and blindness, and degenerative changes in the joints; sensorineural deafness may also occur. It resembles… …   Medical dictionary

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