Literature DB >> 15520787

Purine nucleoside phosphorylase deficiency (PNP-def) presenting with lymphopenia and developmental delay: successful correction with umbilical cord blood transplantation.

Laurie A Myers1, Michael S Hershfield, Wirt T Neale, Maria Escolar, Joanne Kurtzberg.   

Abstract

Purine nucleoside phosphorylase deficiency is a primary immunodeficiency syndrome characterized by the triad of recurrent infection, neurologic dysfunction, and autoimmunity. This patient presented atypically with few infections and normal T-cell function. Progressive lymphopenia, ataxia, and developmental delay led to diagnosis. Umbilical cord blood transplantation corrected the immunodeficiency.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15520787     DOI: 10.1016/j.jpeds.2004.06.075

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  13 in total

1.  Purine nucleoside phosphorylase deficiency with a novel PNP gene mutation: a first case report from India.

Authors:  Manisha Rajan Madkaikar; Shilpa Kulkarni; Prashant Utage; Lynette Fairbanks; Kanjaksha Ghosh; Anthony Marinaki; Mukesh Desai
Journal:  BMJ Case Rep       Date:  2011-12-08

Review 2.  CoQ(10) deficiencies and MNGIE: two treatable mitochondrial disorders.

Authors:  Michio Hirano; Caterina Garone; Catarina M Quinzii
Journal:  Biochim Biophys Acta       Date:  2012-01-18

Review 3.  Untying the Gordian knot: policies, practices, and ethical issues related to banking of umbilical cord blood.

Authors:  Joanne Kurtzberg; Anne Drapkin Lyerly; Jeremy Sugarman
Journal:  J Clin Invest       Date:  2005-10       Impact factor: 14.808

4.  Cross correction following haemopoietic stem cell transplant for purine nucleoside phosphorylase deficiency: engrafted donor-derived white blood cells provide enzyme to residual enzyme-deficient recipient cells.

Authors:  Vikramajit Singh
Journal:  JIMD Rep       Date:  2012-03-02

5.  Hematopoietic cell transplantation for a child with OSTM1 osteopetrosis.

Authors:  Kathleen M Overholt; Melissa J Rose; Sarita Joshi; Gail E Herman; Rajinder Bajwa; Rolla Abu-Arja; Hemalatha G Rangarajan; Edwin M Horwitz
Journal:  Blood Adv       Date:  2016-12-30

6.  TAT-mediated intracellular delivery of purine nucleoside phosphorylase corrects its deficiency in mice.

Authors:  Ana Toro; Eyal Grunebaum
Journal:  J Clin Invest       Date:  2006-09-07       Impact factor: 14.808

7.  Novel Genetic Mutations in the First Swedish Patient with Purine Nucleoside Phosphorylase Deficiency and Clinical Outcome After Hematopoietic Stem Cell Transplantation with HLA-Matched Unrelated Donor.

Authors:  Nicholas Brodszki; Maria Svensson; André B P van Kuilenburg; Judith Meijer; Lida Zoetekouw; Lennart Truedsson; Jacek Toporski
Journal:  JIMD Rep       Date:  2015-05-13

Review 8.  Inborn errors of metabolism underlying primary immunodeficiencies.

Authors:  Nima Parvaneh; Pierre Quartier; Parastoo Rostami; Jean-Laurent Casanova; Pascale de Lonlay
Journal:  J Clin Immunol       Date:  2014-08-01       Impact factor: 8.317

9.  Upfront Enzyme Replacement via Erythrocyte Transfusions for PNP Deficiency.

Authors:  Anna Eichinger; Horst von Bernuth; Michael H Albert; Fabian Hauck; Cinzia Dedieu; Sebastian A Schroeder; Giancarlo la Marca
Journal:  J Clin Immunol       Date:  2021-02-27       Impact factor: 8.317

10.  The Broad Clinical Spectrum and Transplant Results of PNP Deficiency.

Authors:  Polina Stepensky; Irina Zaidman; Yael Dinur Schejter; Ehud Even-Or; Bella Shadur; Adeeb NaserEddin
Journal:  J Clin Immunol       Date:  2019-11-09       Impact factor: 8.542

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.