![A prenatally diagnosed case of Donnai‐Barrow syndrome: Highlighting the importance of whole exome sequencing in cases of consanguinity - Ozdemir - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library A prenatally diagnosed case of Donnai‐Barrow syndrome: Highlighting the importance of whole exome sequencing in cases of consanguinity - Ozdemir - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/178fda7e-8dbd-4cf8-933c-b98ef042fd8e/ajmga61428-fig-0001-m.jpg)
A prenatally diagnosed case of Donnai‐Barrow syndrome: Highlighting the importance of whole exome sequencing in cases of consanguinity - Ozdemir - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
![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
![PDF) Umblical hernia, hypertelorism, sensorineural deafness: Is it Donnai� Barrow syndrome? | Ersel Onrat - Academia.edu PDF) Umblical hernia, hypertelorism, sensorineural deafness: Is it Donnai� Barrow syndrome? | Ersel Onrat - Academia.edu](https://0.academia-photos.com/attachment_thumbnails/41389934/mini_magick20190219-13800-eu0ohk.png?1550597223)
PDF) Umblical hernia, hypertelorism, sensorineural deafness: Is it Donnai� Barrow syndrome? | Ersel Onrat - Academia.edu
![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.
![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
![Induced pluripotent stem cell-based disease modeling identifies ligand-induced decay of megalin as a cause of Donnai-Barrow syndrome - ScienceDirect Induced pluripotent stem cell-based disease modeling identifies ligand-induced decay of megalin as a cause of Donnai-Barrow syndrome - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0085253820302635-fx1.jpg)
Induced pluripotent stem cell-based disease modeling identifies ligand-induced decay of megalin as a cause of Donnai-Barrow syndrome - ScienceDirect
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
![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
![Patient 1. a: Note hypertelorism, marked underorbital creases, short... | Download Scientific Diagram Patient 1. a: Note hypertelorism, marked underorbital creases, short... | Download Scientific Diagram](https://www.researchgate.net/publication/10609532/figure/fig3/AS:267698424774698@1440835686481/Patient-1-a-Note-hypertelorism-marked-underorbital-creases-short-nose-with-broad-tip.png)
Patient 1. a: Note hypertelorism, marked underorbital creases, short... | Download Scientific Diagram
![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/70cbf2ec-c7f0-4d3a-8bbf-f63211cec4a1/mfig002.jpg)
Donnai‐Barrow syndrome: Four additional patients - Chassaing - 2003 - American Journal of Medical Genetics Part A - Wiley Online Library
![A 56-year-old female patient with facio-oculo-acoustico-renal syndrome (FOAR) syndrome. Report on the natural history and of a novel mutation. | Semantic Scholar A 56-year-old female patient with facio-oculo-acoustico-renal syndrome (FOAR) syndrome. Report on the natural history and of a novel mutation. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/8fc953b5795da30e288a4249c533443584f29280/2-Figure1-1.png)
A 56-year-old female patient with facio-oculo-acoustico-renal syndrome (FOAR) syndrome. Report on the natural history and of a novel mutation. | Semantic Scholar
![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/9cc3ffbf-6911-40d2-976a-bf7f73c9fba1/mfig003.jpg)
Donnai‐Barrow syndrome: Four additional patients - Chassaing - 2003 - American Journal of Medical Genetics Part A - Wiley Online Library
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Variable expression pattern in Donnai-Barrow syndrome: Report of two novel LRP2 mutations and review of the literature - ScienceDirect
![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)