Primary care
Recommendation 1
Symptomatic and supportive
Agenesis of Corpus Callosum
Not yet reviewedThis information is AI generated and has not yet been reviewed by a specialist physician. AI can make mistakes.
Disease overview
A rare congenital disorder lacking development of the corpus callosum, the structure which connects the two brain hemispheres
Common symptoms
Most common are epileptic seizuresfeeding problemsdelays in holding the head erectimpairment of mental and physical developmentand hydrocephalus. [ ]
When to suspect
Recommendation 1
Ultrasound and MRI
How to test
Recommendation 1
Ultrasound and MRI
ZebraMD is partnering with Ambry Genetics for clinical-grade whole genome testing for rare diseases. Ambry accepts insurance. If you don’t have a physician to order this test, join our referral list and our team will reach out.
Treatment
Recommendation 1
Symptomatic and supportive
Further support
Recommendation 1
None currently available. . Referral to Medical Genetics Department, if available. Initial virtual care is also available through organizations like TeleRare Health.
Clinical trials
Clinical Trials
Sources
No data available
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