Biometry, optical coherence tomography, and further clinical observations in Knobloch syndrome
Author:
Affiliation:
1. Division of Pediatric Ophthalmology, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia
2. Eye Institute, Cleveland Clinic Abu Dhabi, Abu Dhabi, United Arab Emirates
Publisher
Informa UK Limited
Subject
Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health
Link
https://www.tandfonline.com/doi/pdf/10.3109/13816810.2016.1164197
Reference25 articles.
1. Congenital scalp defects and vitreoretinal degeneration: Redefining the Knobloch syndrome
2. The second report of Knobloch syndrome
3. Knobloch syndrome in a large Brazilian consanguineous family: Confirmation of autosomal recessive inheritance
4. Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome)
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