Stickler Syndrome Type 1 with Short Stature and Atypical Ocular Manifestations

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...

Full description

Saved in:
Bibliographic Details
Main Authors: Manisha Goyal, Seema Kapoor, Shiro Ikegawa, Gen Nishimura
Format: Article
Language:English
Published: Wiley 2016-01-01
Series:Case Reports in Pediatrics
Online Access:http://dx.doi.org/10.1155/2016/3198597
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items

Similar Items