Developmental dysphasia familial
- Other Names:
Developmental language disorder; Specific language impairmentDevelopmental language disorder; Specific language impairment
Many rare diseases have limited information. Currently GARD is able to provide the following information for this disease:
This section is currently in development.
All individuals inherit two copies of most genes. The number of copies of a gene that need to have a disease-causing variant affects the way a disease is inherited. This disease is inherited in the following pattern(s):
Describe details about the symptoms. Because there may be many different causes for a single symptom, it is best not to make a conclusion about the diagnosis. The detailed descriptions help the medical provider determine the correct diagnosis.
To help describe a symptom:
Working with a medical team to find a diagnosis can be a long process that will require more than one appointment. Make better health decisions by being prepared for the first visit with each member of the medical team.
Last Updated: Nov. 8, 2021