Clinical and molecular analysis of three Mexican families with Pendred's syndrome

Ofelia González Treviño, Onur K. Arseven, CJ Ceballos, VI Vives, RC Ramirez, V Fuentes Gómez, Geraldo Medeiros‐Neto, Peter Kopp

European Journal of Endocrinology · 2001 · 60 citations · 26 references

Abstract

All patients included in this study presented with the classic Pendred syndrome triad and molecular analysis revealed pendrin mutations as the underlying cause. The identification of three novel mutations, one of them of complex structure, expands the spectrum of mutations in the PDS gene and emphasizes that they display marked allelic heterogeneity.

References

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