Bardet-Biedl syndrome.

Authors

  • Luís Siopa Serviço de Medicina 2, Hospital Distrital de Santarém, Santarém.
  • Manuela Grego
  • Joel Cossa
  • Alberto Pinguinha

DOI:

https://doi.org/10.20344/amp.1905

Abstract

Bardet-Biedl syndrome is a rare disease characterized by pigmentary retinopathy, dysmorphic extremities, obesity, renal abnormalities and hypogonadism only in men. The authors present a typical case and made a brief commentary about the disease's cardinal manifestations.

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How to Cite

1.
Siopa L, Grego M, Cossa J, Pinguinha A. Bardet-Biedl syndrome. Acta Med Port [Internet]. 2002 Feb. 27 [cited 2024 Nov. 13];15(1):51-4. Available from: https://actamedicaportuguesa.com/revista/index.php/amp/article/view/1905

Issue

Section

Arquivo Histórico