non-syndromic X-linked intellectual developmental disorder 111

A non-syndromic X-linked intellectual disability characterized by different degrees of impaired intellectual development associated with motor, speech and behavioral impairments that has_material_basis_in hemizygous or heterozygous mutation in the SLITRK2 gene

A non-syndromic X-linked intellectual disability characterized by different degrees of impaired intellectual development associated with motor, speech and behavioral impairments that has_material_basis_in hemizygous or heterozygous mutation in the SLITRK2 gene on chromosome Xq27.

Signs and symptoms

• Global developmental delay
• Intellectual disability
• Anxiety
• Unsteady gait
• Delayed speech and language development
• Kyphoscoliosis
• Feeding difficulties
• Reduced cerebral white matter volume
• Autistic behavior
• Seizure

Also known as: XLID111