![Stream episode Episode 53: Lauricia- Cornelia De Lange Syndrome by Orange Socks podcast | Listen online for free on SoundCloud Stream episode Episode 53: Lauricia- Cornelia De Lange Syndrome by Orange Socks podcast | Listen online for free on SoundCloud](https://i1.sndcdn.com/artworks-000229309569-8jylwh-t500x500.jpg)
Stream episode Episode 53: Lauricia- Cornelia De Lange Syndrome by Orange Socks podcast | Listen online for free on SoundCloud
Bonsoir ! Quelques nouvelles de Mya ! Alors premièrement, ses prélèvements sanguins n'ont rien donné d'alarmant. Du coup, on a amélioré son "régime" alimentaire en ajoutant plus de féculents et en augmentant
Madmoiz'elle Mya: son quotidien avec le syndrome cornelia de lange. - Bonsoir !! Mya passe de bonnes vacances ! Entre journée grasse mat', grosse sieste Et levé très tôt mais zéro sieste
CENTOGENE - Did you know? #DUK Cornelia de Lange #Didyouknow Cornelia de Lange syndrome (CdLS) is a syndromic disorder, with symptoms that include distinctive facial features including arched eyebrows that often meet
![The characteristic craniofacial features of Cornelia de Lange syndrome. | Download Scientific Diagram The characteristic craniofacial features of Cornelia de Lange syndrome. | Download Scientific Diagram](https://www.researchgate.net/publication/234100200/figure/fig5/AS:324129615040526@1454289930690/The-characteristic-craniofacial-features-of-Cornelia-de-Lange-syndrome.png)
The characteristic craniofacial features of Cornelia de Lange syndrome. | Download Scientific Diagram
![A novel mutation in NIPBL3 in a case of Cornelia de Lange syndrome confirmed with genetic testing following intrauterine fetal death | Journal of Clinical Pathology A novel mutation in NIPBL3 in a case of Cornelia de Lange syndrome confirmed with genetic testing following intrauterine fetal death | Journal of Clinical Pathology](https://jcp.bmj.com/content/jclinpath/67/3/283/F1.large.jpg)
A novel mutation in NIPBL3 in a case of Cornelia de Lange syndrome confirmed with genetic testing following intrauterine fetal death | Journal of Clinical Pathology
![Rare form of autosomal dominant familial Cornelia de Lange syndrome due to a novel duplication in SMC3 - Infante - 2017 - Clinical Case Reports - Wiley Online Library Rare form of autosomal dominant familial Cornelia de Lange syndrome due to a novel duplication in SMC3 - Infante - 2017 - Clinical Case Reports - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/be233542-5b59-43db-b131-fbeac927660a/ccr31010-fig-0001-m.jpg)
Rare form of autosomal dominant familial Cornelia de Lange syndrome due to a novel duplication in SMC3 - Infante - 2017 - Clinical Case Reports - Wiley Online Library
![Medicina | Free Full-Text | De novo NIPBL Mutations in Vietnamese Patients with Cornelia de Lange Syndrome Medicina | Free Full-Text | De novo NIPBL Mutations in Vietnamese Patients with Cornelia de Lange Syndrome](https://www.mdpi.com/medicina/medicina-56-00076/article_deploy/html/images/medicina-56-00076-g001.png)