Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8690924 | Seminars in Pediatric Neurology | 2018 | 6 Pages |
Abstract
In patients presenting with global developmental day, eliciting a history of consanguinity may increase a clinician׳s bias toward suspecting an autosomal recessive etiology. We present 3 cases wherein children of consanguineous parents presented to the pediatric neurology clinic for evaluation and potential diagnosis of the cause of global developmental delay. The outcome of the investigations in each case demonstrate the need to follow established guidelines for appropriate genetic testing as they pertain to the patient׳s presentation rather than a single element of the history (ie, consanguinity).
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Authors
Salva BSC, MD, Michael MDCM, FRCPC, FCAHS,