Conditions / Syndrome
Allan-Herndon-Dudley syndrome
info · Syndrome
A syndrome that has_material_basis_in mutation in the MCT8 gene on chromosome Xq13.
Signs and symptoms
- Narrow forehead
- Clonus
- Delayed CNS myelination
- Inability to walk
- Flexion contracture
- Ataxia
- Severe intellectual disability
- Irritability
- Hallux valgus
- Feeding difficulties in infancy
Also known as: AHDS; ALLAN-HERNDON SYNDROME