FAQ
- Who do you call to make an appointment in the outpatient Genetics clinic?
A: For outpatient appointments, patients can call (909) 835 1899. - What is the procedure for referring a patient?
A: We ask that the referring physician send all pertinent medical records on the patient. If there is a diagnosis known, records documenting the diagnosis must be sent. They can be faxed to (909) 835 1780. The records will be reviewed and further evaluations and/or testing will be recommended as necessary, which are to be done PRIOR TO scheduling the patient’s appointment. - What are some of the tests that Genetics may request prior to setting up the appointment?
A: That depends on the reason for referral. For example, we request a chromosome analysis and/or array CGH on babies with birth defects/ growth problems/ developmental delays. We request cardiology and ophthalmology consultations on patients referred for possible Marfan syndrome. We ask for a skeletal survey on patients referred for a skeletal dysplasia. - What is an array CGH?
A: An array comparative genomic hybridization test checks for missing or extra pieces of chromosome material (deletions and duplications) that are too small to be picked up on routine chromosome analysis. - How can we order an array CGH?
A: An array comparative genomic hybridization or array CGH testing is requested on some patients with multiple congenital anomalies and/ or developmental problems or autism. Based on the patient’s insurance, the testing can be sent to the Mayo Medical Labs (test code 88898), Quest Diagnostics (ClariSure assay 16135X) or LabCorp (SNP microarray test code 510002). - How long is the waiting period for an appointment in the outpatient clinic?
A: The waiting period depends to a large extent on the reason for referral and whether the evaluations/tests requested have been done.
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