📂 Diseases
Meier-Gorlin syndrome 5 — Definition
Meier-Gorlin sendromu tip 5 / Meier-Gorlin syndrome 5
Meier-Gorlin syndrome type 5 is a rare genetic disease, showing autozomal resessive transition. Basic clinical findings include prenatal and post-natal growth backrest, micrognati (small jaw) and pathogen (design cover) absence or hypoplasia. This syndrome is caused by mutations in GMNN gene and leads to disorder in cell cycle editing.
Frequently Asked Questions
❓ What is Meier-Gorlin sendromu tip 5?
Meier-Gorlin sendromu tip 5; meier-Gorlin syndrome type 5 is a rare genetic disease, showing autozomal resessive transition. Basic clinical findings include prenatal and post-natal growth backrest, micrognati (small jaw) and pathogen (design cover) absence or hypoplasia. This syndrome is caused by mutations in GMNN gene and leads to disorder in cell cycle editing.
❓ What is Meier-Gorlin syndrome 5 in Turkish?
The Turkish equivalent of "Meier-Gorlin syndrome 5" is Meier-Gorlin sendromu tip 5.
❓ Which medical field is Meier-Gorlin sendromu tip 5 related to?
This term belongs to the Diseases category.