[Pigmentosum retinis and tubulo-interstitial nephronophtisis in Sensenbrenner syndrome: a case report].

Abstract

PURPOSE Sensenbrenner syndrome or cranio-ectodermal dysplasia is an extremely rare autosomal recessive condition (12 cases reported in literature). Our observation shows the possibility of both ocular and renal involvement associated with cranio-ectodermal abnormalities. PATIENTS and method:We report the case of a girl who presented a typical cranio… (More)

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Cite this paper

@article{Costet2000PigmentosumRA, title={[Pigmentosum retinis and tubulo-interstitial nephronophtisis in Sensenbrenner syndrome: a case report].}, author={C Costet and Fr{\'e}d{\'e}ric B{\'e}tis and {\'E}tienne B{\'e}rard and Michel Tsimaratos and Sabine Sigaudy and Corinne Antignac and Pierre Gastaud}, journal={Journal francais d'ophtalmologie}, year={2000}, volume={23 2}, pages={158-60} }