Woodhouse-Sakati syndrome: a case report

Authors

  • Franklin Aranda Instituto Nacional de Salud del Niño (INSN). Lima, Perú.
  • Miguel Chávez Servicio de Genética, Instituto Nacional de Salud del Niño. Lima, Perú
  • Angel Quispe mauricio Red Asistencial Pasco, Seguro Social de Salud-EsSalud. Pasco, Perú.
  • Adolfo Caro Instituto Nacional de Salud del Niño (INSN). Lima, Perú.

DOI:

https://doi.org/10.15381/anales.v69i4.1126

Keywords:

Woodhouse-Sakati syndrome, receptor, IGF type 1, alopecia, diabetes mellitus, hypogonadism.

Abstract

We present a rare case of Woodhouse-Sakati syndrome in an 11 year-old patient, who presented congenital alopecia, bilateral sensorineural hearing loss, insulindependent diabetes mellitus, primary hypogonadism, psychomotor retardation, interventricular communication, decreased IGF1. The evolution and supportive treatment were satisfactory.

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Published

2008-12-31

Issue

Vol. 69 No. 4 (2008)

Section

Casos clínicos

License

Copyright (c) 2008 Franklin Aranda, Miguel Chávez, Angel Quispe mauricio, Adolfo Caro

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How to Cite

1.
Aranda F, Chávez M, Quispe mauricio A, Caro A. Woodhouse-Sakati syndrome: a case report. An Fac med [Internet]. 2008 Dec. 31 [cited 2024 Jul. 1];69(4):260-2. Available from: https://revistasinvestigacion.unmsm.edu.pe/index.php/anales/article/view/1126