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A rare cause of hydrops fetalis in two Gaucher disease type 2 patients with a novel mutation

Sebile Kılavuz1,2, Murat Basaranoglu3, Serdar Epcacan4

  • 1Division of Pediatric Metabolism and Nutrition, Department of Pediatrics, Van Training and Research Hospital, University of Health Sciences, Van, Turkey. dr.skilavuz@gmail.com.

Metabolic Brain Disease
|March 7, 2022
PubMed

Keywords:
GBAGaucher diseaseIchthyosishydrops fetalis

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