Anomalías congénitas en pacientes azoospérmicos

Authors

  • Guillermo Alemán Souz ECIMED
  • Rubén S. Padrón Durán ECIMED

Abstract

Se estudiaron 135 pacientes con el diagnóstico de azoospermia, en el 12,7% se detectaron una o más anomalías congénitas, las más frecuentes fueron pie plano, cúbito valgo bilateral, paladar ojival y clinodactilia. Todas se presentaron en pacientes con síndrome de Klinefelter, síndrome XX, síndrome YY e hipogonadismo por déficit selectivo de gonadotroplnas. Se concluye que en todo paciente azoospérmico con malformaciones congénitas debe sospecharse un trastorno cromosómico o un hipogonadismo secundario por déficit selectivo de gonadotroplnas; y por tanto, su estudio debe ser orientado sobre la base del diagnóstico de estas enfermedades.

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Published

2020-12-29

How to Cite

1.
Alemán Souz G, Padrón Durán RS. Anomalías congénitas en pacientes azoospérmicos. Rev Cubana Med [Internet]. 2020 Dec. 29 [cited 2025 Mar. 13];24(2). Available from: https://revmedicina.sld.cu/index.php/med/article/view/2307

Issue

Vol. 24 No. 2 (1986)

Section

Original articles

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