📂 Diseases
Meier-Gorlin syndrome 2 — Definition
Meier-Gorlin sendromu 2 / Meier-Gorlin syndrome 2
Meier-Gorlin syndrome 2 is a rare genetic disease, showing autozomal resessive transition. Basic findings include prenatal and post-natal growth backrest, micrognati (small jaw) and pathogen (design cover) absence or hypoplasia. The disease occurs as a result of mutations in the ORC1 gene and leads to disorders in the cell cycle with DNA reapplication. The clinical picture manifests itself with skeleton anomalies and characteristic facial appearance.
Frequently Asked Questions
❓ What is Meier-Gorlin sendromu 2?
Meier-Gorlin sendromu 2; meier-Gorlin syndrome 2 is a rare genetic disease, showing autozomal resessive transition. Basic findings include prenatal and post-natal growth backrest, micrognati (small jaw) and pathogen (design cover) absence or hypoplasia. The disease occurs as a result of mutations in the ORC1 gene and leads to disorders in the cell cycle with DNA reapplication. The clinical picture manifests itself with skeleton anomalies and characteristic facial appearance.
❓ What is Meier-Gorlin syndrome 2 in Turkish?
The Turkish equivalent of "Meier-Gorlin syndrome 2" is Meier-Gorlin sendromu 2.
❓ Which medical field is Meier-Gorlin sendromu 2 related to?
This term belongs to the Diseases category.