Case 1: Microcephaly, Skeletal Dysplasia, and Immunodeficiency in a Newborn
The editors of Pediatrics in Review greatly appreciate feedback from readers, many of whom made it clear that reading the case reports in print form is still preferred. So, in response to your input, this issue takes us "back to the future" with all Index of Suspicion cases again appearing in the print journal as well as online. Thanks for reading, and thanks for the feedback!
Philip R. Fischer, MD Associate Editor, Index of Suspicion
Dr Belal and Ms Malcolmson have disclosed no financial relationships relevant to this article. Dr Day-Salvatore has disclosed that she receives research grant funding for longitudinal studies from Sanofi Genzyme and grant funding from the New Jersey Department of Health Special Child Health and Early Intervention Services. She also serves as a lysosomal storage disease expert for Sanofi Genzyme and receives travel reimbursement and honoraria from the company. This commentary does not contain a discussion of an unapproved/investigative use of a commercial product/device.
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Tarek Belal, Debra-Lynn Day-Salvatore, Janet Malcolmson; Case 1: Microcephaly, Skeletal Dysplasia, and Immunodeficiency in a Newborn. Pediatr Rev July 2018; 39 (7): 359–362. https://doi.org/10.1542/pir.2017-0101
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