A novel mutation in purine nucleoside phosphorylase in a child with normal uric acid levels.

Published

Journal Article

BACKGROUND: Purine nucleoside phosphorylase (PNP) deficiency is an autosomal recessive disease in which affected children present with recurrent infection and may present with failure to thrive, neurological impairment, autoimmunity, or malignancy. The diagnosis of PNP is usually suggested by a reduced level of serum uric acid. We report here a novel mutation in the nucleoside phosphorylase gene (NP gene) in a patient with primary immunodeficiency and neurological impairment but with normal uric acid levels. The diagnosis was confirmed biochemically and showed a reduced PNP activity, and also by molecular gene analysis. METHODS: A case report and a complete NP gene DNA analysis. RESULT: The sequencing analysis showed a novel homozygous missense mutation, c.487T>C in the NP gene, resulting in a substitution of serine by proline at residue 163 (S163P) in the mature NP protein. CONCLUSION: This NP missense mutation reported here is associated with recurrent infection, developmental delay, and primary immunodeficiency combined with normal uric acid levels in the affected child most likely due to a residual PNP enzyme activity. PNP deficiency causing primary immunodeficiency is still possible, even with normal uric acid levels.

Full Text

Duke Authors

Cited Authors

  • Al-Saud, B; Alsmadi, O; Al-Muhsen, S; Al-Ghonaium, A; Al-Dhekri, H; Arnaout, R; Hershfield, MS; Al-Mousa, H

Published Date

  • November 2009

Published In

Volume / Issue

  • 42 / 16-17

Start / End Page

  • 1725 - 1727

PubMed ID

  • 19733163

Pubmed Central ID

  • 19733163

Electronic International Standard Serial Number (EISSN)

  • 1873-2933

Digital Object Identifier (DOI)

  • 10.1016/j.clinbiochem.2009.08.017

Language

  • eng

Conference Location

  • United States