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Stickler Syndrome Type 1 with Short Stature and Atypical Ocular Manifestations

Stickler syndrome or hereditary progressive arthroophthalmopathy is a heterogeneous group of collagen tissue disorders, characterized by orofacial features, ophthalmological features (high myopia, vitreoretinal degeneration, retinal detachment, and presenile cataracts), hearing impairment, mild spon...

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Detalles Bibliográficos
Autores principales:	Goyal, Manisha, Kapoor, Seema, Ikegawa, Shiro, Nishimura, Gen
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi Publishing Corporation 2016
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5149639/ https://www.ncbi.nlm.nih.gov/pubmed/28018693 http://dx.doi.org/10.1155/2016/3198597

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