Fatma Nisa Esen

1 Introduction Interstitial deletions involving the long arm of chromosome 3q, particularly within bands 3q26–3q28, have been associated with a distinctive pattern of developmental abnormalities, including intrauterine growth restriction (IUGR), postnatal short stature, microcephaly, facial dysmorphism, and neurodevelopmental delay (Bouman et al. 2015; Dasouki et al. 2014; Mandrile et al. 2013; Ounap et al. 2016; Robilliard and Caylan 2020; Sahin et al. 2014; Tolezano et al. 2024; Zarate et al. 2013).

1 Introduction Rhabdomyolysis is a severe medical condition characterized by the breakdown of skeletal muscle fibers, resulting in the release of muscle cell contents into the bloodstream. This process can lead to complications such as acute kidney injury, electrolyte imbalances, and disseminated intravascular coagulation (Scalco et al. 2015). The etiology of rhabdomyolysis is multifactorial, including traumatic, exertional, metabolic, infectious, toxic, and genetic causes.