Diabetes mellitus en contexto de enfermedad mitocondrial fenotipo Kearns-Sayre

Authors

  • Carmen Yllera-Gutiérrez Servicio de Medicina Interna, Hospital Universitario Central de Asturias, Oviedo (Asturias), Spain
  • Carlota Argüello-Martín Servicio de Medicina Interna, Hospital Universitario Central de Asturias, Oviedo (Asturias), Spain
  • Lucía Meijide-Rodríguez Servicio de Medicina Interna, Hospital Universitario Central de Asturias, Oviedo (Asturias), Spain
  • María Folgueras-Gómez Servicio de Medicina Interna, Hospital Universitario Central de Asturias, Oviedo (Asturias), Spain
  • Silvia Suárez-Díaz Servicio de Medicina Interna, Hospital Universitario Central de Asturias, Oviedo (Asturias), Spain

DOI:

https://doi.org/10.32818/reccmi.a4s1a2

Keywords:

mitochondrial disease, Kearns-Sayre Syndrome, diabetes mellitus

Abstract

A 36-year-old female patient with history of diabetes mellitus, sensorineural hearing loss and pigmentary retinosis. She was diagnosed of mitochondrial myopathy, phenotype Kearns-Sayre syndrome after consulting for long-term palpebral ptosis and progresive muscle weakness. Endocrinopathies are frecuent in this syndrome, based on energy deficit for hormonal secretion. She passed away after multiples heart failure episodes because of miocardial afection, though typical afection in Kearns-Sayre syndrome is on branch conduction pathaways.

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References

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Laloi-Michelin M, Virally M, Jardel C, Meas T, Ingster-Moati I, Lombès A, et al. Kearns-Sayre syndrome: an unusual form of mitochondrial diabetes. Diabetes Metab. 2006 Apr; 32(2): 182-186. doi: https://doi.org/10.1016/S1262-3636(07)70267-7.4.

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Published

2019-01-31

How to Cite

1.
Yllera-Gutiérrez C, Argüello-Martín C, Meijide-Rodríguez L, Folgueras-Gómez M, Suárez-Díaz S. Diabetes mellitus en contexto de enfermedad mitocondrial fenotipo Kearns-Sayre. Rev Esp Casos Clin Med Intern [Internet]. 2019 Jan. 31 [cited 2024 Dec. 4];4:3-4. Available from: https://www.reccmi.com/RECCMI/article/view/353