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English

The onset of clinical manifestations of this patient, even in childhood, coincides with the literature, since the KSS is characterized by ophthalmoplegia and pigmentary retinopathy, usually manifests before the age of twenty; however other changes are associated in several published case reports such as protein concentration, proximal myopathy, thyroid disorders, hypoparathyroidism, Addison’s disease, dysphasia in achalasia and renal tubular acidosis, short stature, cerebellar ataxia and cardiac conduction disturbance were also identified in the case reported3,6,8.

Spanish

El inicio de las manifestaciones clínicas de este paciente, incluso en la infancia, coincide con la literatura, ya que el SKS se caracteriza por oftalmoplejía y retinopatía pigmentaria, por lo general, antes de los 20 años de edad; existiendo otras alteraciones asociadas en varios informes de casos en la literatura, tales como: ataxia cerebelosa, alteración de la conducción cardíaca, hiperproteinorraquia, miopatía durante la penetración del óvulo.