hrp0098p2-202 | Multisystem Endocrine Disorders | ESPE2024
Daka Ayman
, Lahav Einat
, Bar-Yosef Omer
, Bolkier Yoav
, Levy-Shraga Yael
, Anikster Yair
, Jacoby Elad
, Gruber Noah
Background: Mitochondrial disorders resulting from single large-scale mitochondrial DNA (mtDNA) deletions (SLSMDs) are a group of non-inherited congenital diseases that lead to three clinically overlapping syndromes: Pearson syndrome (PS), Kearns-Sayre syndrome (KSS), and chronic progressive external ophthalmoplegia (PEO). Although many reports have addressed endocrine abnormalities in patients with SLSMD, there hasn't been an in-depth study on these abno...