Conditions / Syndrome
Meier-Gorlin syndrome 6
info · Syndrome
A Meier-Gorlin syndrome that has_material_basis_in heterozygous mutation in the GMNN gene on chromosome 6p22.
Signs and symptoms
- Severe short stature
- Thick vermilion border
- Microtia
- Delayed skeletal maturation
- Underdeveloped nasal alae
- Feeding difficulties
- Small for gestational age
- Microretrognathia
- Patellar aplasia
- Frontal bossing