Conditions / Syndrome
Meier-Gorlin syndrome 2
info · Syndrome
A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ORC4 gene on chromosome 2q23.
Signs and symptoms
- Short stature
- Narrow mouth
- Microtia
- Delayed skeletal maturation
- Birth length less than 3rd percentile
- Breast hypoplasia
- Feeding difficulties
- Slender long bone
- Micrognathia
- Microcephaly