Novel mutation in the nephrin gene of a Japanese patient with congenital nephrotic syndrome of the Finnish type.

Department of Pediatrics, Okayama University Medical School, Okayama, Japan.

BACKGROUND: Congenital nephrotic syndrome (CNS) of the Finnish type is a rare autosomal-recessive disorder. Kestila et al reported that a positionally cloned gene for a novel glomerular protein nephrin is mutated in CNS. Most Finnish patients have one of two mutations. In this study, we described a Japanese CNS family associated with a novel missense point mutation in the nephrin gene. METHODS: Reverse transcription-polymerase chain reaction, polymerase chain reaction, and sequence analysis were used. RESULTS: The patient had the three missense mutations homozygously. One mutation was already reported as sequence variant. The two other novel mutations were the GAG to AAG transition, leading to a Glu447Lys and the GAC to GTC transition, predicting an Asp819Val substitution in the nephrin protein. CONCLUSION: Our findings indicate that an abnormality of nephrin may cause CNS of the Finnish type in Japanese subjects.

PMID: 10652016 [PubMed - indexed for MEDLINE]