The Board has remanded the case due to insufficient development regarding the etiology of the Veteran's strokes and their connection to service, specifically exposure to herbicide agents. The Veteran is presumed exposed to herbicide agents but his gene mutation causing stroke is not known to be related to such exposure.
The deciding factor: The examiner must determine if the Veteran’s heterozygous gene mutation to prothrombin with antithrombin III deficiency is acquired and whether it is related to service, specifically exposure to herbicide agents.
- Claimed conditions
- residuals of stroke
- How they argued it
- Not specified
- Exposure basis
- None
- Rating assigned
- None in this decision
- Decision date
- April 10, 2020
- Citation
- 20024982
This is a plain-language summary generated by AI from a public Board of Veterans’ Appeals decision. It can contain errors — always verify against the original. Look up the original decision on VA.gov (opens in a new tab) using citation 20024982.
What this means for you
A remand is not a loss. The Board sent the case back for more development — often a new exam or missing records — before making a final decision. Many remands later end in a grant, and the decision spells out exactly what the Board wanted to see.
What you can do next
Related decisions
Other Board decisions on a similar condition or argued the same way.
- Granted
The Board granted service connection for residuals of stroke, as secondary to the Veteran's service-connected intermittent explosive disorder.
- Remanded (sent back)
The Board remands the claims for service connection for a psychiatric disorder, heart disorder, residuals of stroke, and obstructive sleep apnea to correct duty to assist errors.
- Granted
The Board granted an effective date of January 31, 2022, for service connection for hypertension and residuals of a stroke.
- Partly granted
The Board granted service connection for hypertension, residuals of stroke, and osteoarthritis right hip including right thigh injury. The Veteran's disability rating in excess of 40 percent for osteoarthritis and degenerative disc disease of lumbar spine was denied.
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