Example Study Recommendation Letter #1 (Pediatric) Page 2

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massively parallel sequencing was obtained for [patient name] and was unrevealing.
At this time, we are unable to identify a specific genetic etiology that would explain the findings
seen in [patient name] and [patient name]. The presentation of two siblings with similar features,
however, is suggestive of a possible autosomal recessive condition, which remains undiagnosed
at this time. Parents are interested in identifying a diagnosis, and are also interested in having a
third child. We would like to refer these siblings to the Undiagnosed Diseases Network for further
evaluation to try and identify a diagnosis. Thank you for your review and consideration for
acceptance into the program. Please do not hesitate to contact our office at [phone number] if
you have any questions or require any additional materials.
Sincerely,
Healthcare provider signature
[Healthcare provider name]
Letter #1, Page 2

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