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Case report
Novel NSDHL gene variant for congenital hemidysplasia with ichthyosiform erythroderma and limb defects (CHILD) syndrome

Authors

  • Ebner Bon Gatus Maceda Division of Clinical Genetics, Department of Pediatrics, Philippine General Hospital, University of the Philippines Manila, Manila, Philippines PubMed articlesGoogle scholar articles
  • Lisa E Kratz Biochemical Genetics Laboratory, Kennedy Krieger Institute, Baltimore, Maryland, USA PubMed articlesGoogle scholar articles
  • Veronica Marie E Ramos Dermatology, University of the Philippines Manila, Manila, Philippines PubMed articlesGoogle scholar articles
  • Mary Ann R Abacan Division of Clinical Genetics, Department of Pediatrics, Philippine General Hospital, University of the Philippines Manila, Manila, PhilippinesInstitute of Human Genetics, National Institutes of Health, University of the Philippines Manila, Manila, Philippines PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Ebner Bon Gatus Maceda; egmaceda{at}up.edu.ph
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Citation

Maceda EBG, Kratz LE, Ramos VME, et al
Novel NSDHL gene variant for congenital hemidysplasia with ichthyosiform erythroderma and limb defects (CHILD) syndrome

Publication history

  • Accepted September 21, 2020
  • First published November 2, 2020.
Online issue publication 
November 02, 2020

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