A Novel PGM3 Mutation Is Associated With a Severe Phenotype of Bone Marrow Failure, Severe Combined Immunodeficiency, Skeletal Dysplasia, and Congenital Malformations. (26th June 2017)

• Record Type: Journal Article
• Authors: Pacheco‐Cuéllar, Guillermo; Gauthier, Julie; Désilets, Valérie; Lachance, Christian; Lemire‐Girard, Marlène; Rypens, Françoise; Le Deist, Françoise; Decaluwe, Hélène; Duval, Michel; Bouron‐Dal Soglio, Dorothée; Kokta, Victor; Haddad, Élie; Campeau, Philippe M
• Is Part Of: Journal of bone and mineral research. Volume 32:Number 9(2017:Sep.)
• Page Start: 1853
• Page End: 1859
• Publication Date: 2017-06-26
• Subjects: PGM3 -- BONE MARROW FAILURE -- SEVERE COMBINED IMMUNODEFICIENCY -- CONGENITAL DISORDER OF GLYCOSYLATION -- DESBUQUOIS‐LIKE DYSPLASIA -- WHOLE‐EXOME SEQUENCING; Bones -- Metabolism -- Periodicals; Mineral metabolism -- Periodicals; 612.392
• DOI: 10.1002/jbmr.3173
• Languages: English
• ISSNs: 0884-0431

Abstract

ABSTRACT: Congenital disorders of glycosylation (CDGs) affect multiple systems and present a broad spectrum of clinical features, often including skeletal dysplasia. Exome sequencing has led to the identification of new CDG genes. Immune and skeletal phenotypes associated with mutations in PGM3, encoding a protein that converts N‐acetyl‐glucosamine‐6‐phosphate into N‐acetyl‐glucosamine‐1‐phosphate, were recently reported. Through exome sequencing, we identified a novel homozygous mutation (c.1135T>C; p.Phe379Leu) in PGM3 in two siblings with bone marrow failure, severe combined immunodeficiency, renal and intestinal malformations, and a skeletal dysplasia resembling Desbuquois dysplasia. Severe respiratory compromise secondary to lung hypoplasia and pulmonary hypertension, and intestinal obstruction led to their demise. We thus report the most severe phenotype described so far associated with PGM3 mutations. This CDG should be considered in the presence of skeletal dysplasia associated with severe immunodeficiency. © 2017 American Society for Bone and Mineral Research.