Response to Zhang et al

Sarah J Hart¹, Kanecia Zimmerman², Corinne M Linardic^{2

3}, Sheila Cannon⁴, Anna Pastore⁵, Vasiliki Patsiogiannis⁶, Paolo Rossi^{5

7}, Stephanie L Santoro^{6

8

9}, Brian G Skotko^{6

9}, Amy Torres⁶, Diletta Valentini⁷, Kishore Vellody⁴, Gordon Worley², Priya S Kishnani²

Affiliations

¹ Department of Pediatrics, Duke University Medical Center, Durham, NC, USA. sarah.hart@duke.edu.
² Department of Pediatrics, Duke University Medical Center, Durham, NC, USA.
³ Department of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC, USA.
⁴ Down Syndrome Center of Western Pennsylvania, University of Pittsburgh Medical Center Children's Hospital of Pittsburgh, Pittsburgh, PA, USA.
⁵ Laboratory of Molecular Genetics and Functional Genomics, Division of Genetic and Rare Disease, Bambino Gesù Children's Hospital and Research Institute, Rome, Italy.
⁶ Down Syndrome Program, Division of Medical Genetics and Metabolism, Department of Pediatrics, Massachusetts General Hospital, Rome, Italy.
⁷ Department of Pediatrics, Bambino Gesù Children's Hospital and Research Institute, Rome, Italy.
⁸ Division of Genetics, Nationwide Children's Hospital, Columbus, OH, USA.
⁹ Department of Pediatrics, Harvard Medical School, Boston, MA, USA.

Free article

Comment

Sarah J Hart et al. Genet Med. 2020 Mar.

Free article

. 2020 Mar;22(3):662.

doi: 10.1038/s41436-019-0690-z. Epub 2019 Nov 12.

¹ Department of Pediatrics, Duke University Medical Center, Durham, NC, USA. sarah.hart@duke.edu.
² Department of Pediatrics, Duke University Medical Center, Durham, NC, USA.
³ Department of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC, USA.
⁴ Down Syndrome Center of Western Pennsylvania, University of Pittsburgh Medical Center Children's Hospital of Pittsburgh, Pittsburgh, PA, USA.
⁵ Laboratory of Molecular Genetics and Functional Genomics, Division of Genetic and Rare Disease, Bambino Gesù Children's Hospital and Research Institute, Rome, Italy.
⁶ Down Syndrome Program, Division of Medical Genetics and Metabolism, Department of Pediatrics, Massachusetts General Hospital, Rome, Italy.
⁷ Department of Pediatrics, Bambino Gesù Children's Hospital and Research Institute, Rome, Italy.
⁸ Division of Genetics, Nationwide Children's Hospital, Columbus, OH, USA.
⁹ Department of Pediatrics, Harvard Medical School, Boston, MA, USA.

No abstract available

Comment on

Detection of iron deficiency in children with Down syndrome.
Hart SJ, Zimmerman K, Linardic CM, Cannon S, Pastore A, Patsiogiannis V, Rossi P, Santoro SL, Skotko BG, Torres A, Valentini D, Vellody K, Worley G, Kishnani PS. Hart SJ, et al. Genet Med. 2020 Feb;22(2):317-325. doi: 10.1038/s41436-019-0637-4. Epub 2019 Aug 16. Genet Med. 2020. PMID: 31417190 Free PMC article.
Detection of iron deficiency in children with Down syndrome.
Zhang WY, Liu YY, Zeng DX. Zhang WY, et al. Genet Med. 2020 Mar;22(3):661. doi: 10.1038/s41436-019-0699-3. Epub 2019 Nov 12. Genet Med. 2020. PMID: 31712671 No abstract available.

1. Zhang W, Liu Y, Zeng, D. Detection of iron deficiency in children with Down syndrome. Genet Med. In Press.
1. Hart SJ, Zimmerman K, Linardic CM, et al. Detection of iron deficiency in children with Down syndrome. Genet Med. 2019 Aug 16; https://doi.org/10.1038/s41436-019-0637-4 [Epub ahead of print]. - DOI
1. Baker RD, Greer FR. Committee on Nutrition American Academy of P. Diagnosis and prevention of iron deficiency and iron-deficiency anemia in infants and young children (0-3 years of age). Pediatrics. 2010;126:1040–50. - DOI
1. Bharadwaj S, Ginoya S, Tandon P, et al. Malnutrition: laboratory markers vs nutritional assessment. Gastroenterol Rep (Oxf). 2016;4:272–80.