![Persistent pupillary membrane, strabismus, and optic nerve hypoplasia in Donnai-Barrow syndrome - ScienceDirect Persistent pupillary membrane, strabismus, and optic nerve hypoplasia in Donnai-Barrow syndrome - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1091853111005301-gr1.jpg)
Persistent pupillary membrane, strabismus, and optic nerve hypoplasia in Donnai-Barrow syndrome - ScienceDirect
![Donnai– Barrow Syndrome in Two Sisters with a Homozygous LRP2 Mutation and Renal Dysfunction. Integral Management of the Disease with Review of the Literature. Donnai– Barrow Syndrome in Two Sisters with a Homozygous LRP2 Mutation and Renal Dysfunction. Integral Management of the Disease with Review of the Literature.](https://www.hilarispublisher.com/articles-images/molecular-genetic-medicine-syndrome-14-451-g001.png)
Donnai– Barrow Syndrome in Two Sisters with a Homozygous LRP2 Mutation and Renal Dysfunction. Integral Management of the Disease with Review of the Literature.
![Michelle Rheault on Twitter: "Donnai-Barrow Syndrome: absence of megalin. #aspn19 https://t.co/bQBlMKQFob https://t.co/LhxNfaTfYV" / Twitter Michelle Rheault on Twitter: "Donnai-Barrow Syndrome: absence of megalin. #aspn19 https://t.co/bQBlMKQFob https://t.co/LhxNfaTfYV" / Twitter](https://pbs.twimg.com/media/D5KVT3mX4AIPDVT.jpg:large)
Michelle Rheault on Twitter: "Donnai-Barrow Syndrome: absence of megalin. #aspn19 https://t.co/bQBlMKQFob https://t.co/LhxNfaTfYV" / Twitter
I am Mylo Black - "Donnai-Barrow syndrome......what?!" That's what my mummy and daddy said when the geneticist told them. Now I will stress, this is a pre-diagnosis and until the tests come
![Donnai–Barrow syndrome (DBS/FOAR) in a child with a homozygous LRP2 mutation due to complete chromosome 2 paternal isodisomy - Kantarci - 2008 - American Journal of Medical Genetics Part A - Wiley Online Library Donnai–Barrow syndrome (DBS/FOAR) in a child with a homozygous LRP2 mutation due to complete chromosome 2 paternal isodisomy - Kantarci - 2008 - American Journal of Medical Genetics Part A - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/7fbc2718-5115-4b48-9aec-f96e2f62242f/mfig001.jpg)
Donnai–Barrow syndrome (DBS/FOAR) in a child with a homozygous LRP2 mutation due to complete chromosome 2 paternal isodisomy - Kantarci - 2008 - American Journal of Medical Genetics Part A - Wiley Online Library
![Phenotype resembling Donnai–Barrow syndrome in a patient with 9qter;16qter unbalanced translocation - Ferrero - 2006 - American Journal of Medical Genetics Part A - Wiley Online Library Phenotype resembling Donnai–Barrow syndrome in a patient with 9qter;16qter unbalanced translocation - Ferrero - 2006 - American Journal of Medical Genetics Part A - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/d14f35dd-122b-4d4a-a898-d4c351918fef/mfig002.jpg)
Phenotype resembling Donnai–Barrow syndrome in a patient with 9qter;16qter unbalanced translocation - Ferrero - 2006 - American Journal of Medical Genetics Part A - Wiley Online Library
![JPM | Free Full-Text | Stickler Syndrome: A Review of Clinical Manifestations and the Genetics Evaluation JPM | Free Full-Text | Stickler Syndrome: A Review of Clinical Manifestations and the Genetics Evaluation](https://www.mdpi.com/jpm/jpm-10-00105/article_deploy/html/images/jpm-10-00105-g001.png)
JPM | Free Full-Text | Stickler Syndrome: A Review of Clinical Manifestations and the Genetics Evaluation
![Donnai‐Barrow syndrome: Four additional patients - Chassaing - 2003 - American Journal of Medical Genetics Part A - Wiley Online Library Donnai‐Barrow syndrome: Four additional patients - Chassaing - 2003 - American Journal of Medical Genetics Part A - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/fed7d338-42f2-43f0-86fa-45882ada961d/mfig001.jpg)