A novel PCFT gene mutation (p.Cys66LeufsX99) causing hereditary folate malabsorption

Esther Meyer, Manju A. Kurian, Shanaz Pasha, Richard C. Trembath, Trevor Cole, Eamonn R. Maher

Research output: Contribution to journalArticlepeer-review

28 Citations (Scopus)

Abstract

Hereditary folate malabsorption (HFM) is a rare autosomal recessive disorder which is characterized by impaired intestinal folate malabsorption and impaired folate transport into the central nervous system. Mutations in the intestinal folate transporter PCFT have been reported previously in only 10 individuals with this disorder. The purpose of the current Study was to describe the clinical phenotype and determine the molecular basis for this disorder in a family with four affected individuals. A consanguineous family of Pakistani origin with autosomal recessive HFM was ascertained and clinically phenotyped. After genetic linkage studies all coding exons of the PCFT gene were screened for mutations by direct sequencing. The clinical phenotype of four affected patients is described. Direct sequencing of PCFT revealed a novel homozygous frameshift mutation (c.194dupG) at a mononucleotide repeat in exon I predicted to result in a truncated protein (p.Cys66LeufsX99). This report extends current knowledge on the phenotypic manifestations of HFM and the PCFT mutation spectrum. (C) 2009 Elsevier Inc. All rights reserved.
Original languageEnglish
Pages (from-to)325 - 328
Number of pages4
JournalMOLECULAR GENETICS AND METABOLISM
Volume99
Issue number3
DOIs
Publication statusPublished - Mar 2010

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