Professionals

Main clinical features
The so far described patients point towards a phenotype, which comprises key symptoms such as expressive speech delay and notable social behavior deficits. At the same time, it demonstrates the broad phenotypic spectrum associated with QRICH1-associated disorders. Enlargement of QRICH1 cohorts is prerequisite to learn in more detail about the range of clinical symptoms

Prevalence
Undetermined

Inheritance
Autosomal dominant