Conditions / Syndrome
Meier-Gorlin syndrome 3
info · Syndrome
A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ORC6 gene on chromosome 16q11.
Signs and symptoms
- Thick vermilion border
- Microtia
- Birth length less than 3rd percentile
- Breast hypoplasia
- Slender long bone
- Hypoplasia of the maxilla
- Intrauterine growth retardation
- Cryptorchidism
- Micrognathia
- Microcephaly