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Polyendocrinopathy and multisystem involvement are common phenotypic features of Kearns-Sayre syndrome

  Dear Editor,   We were interested to read the article by Amergoolov et al. on two patients with Kearns-Sayre Syndrome (KSS) due to single mtDNA deletions who had phenotypic endocrine disorders among other features.1 Patient 1, a 20-year-old female, was diagnosed with hypogonadism, diabetes and...

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Autore principale: Josef Finsterer
Natura: Artigo
Lingua:Inglês
Pubblicazione: PAGEPress Publications 2025-04-01
Serie:European Journal of Translational Myology
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Accesso online:https://www.pagepressjournals.org/bam/article/view/13634
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