Posted inDiabetes & Endocrinology news Pediatrics
Pubertal Delay Associated with Paternally Derived 15q11.2-q13 Duplication Syndrome and MKRN3 Overexpression: A Case Series
This report discusses four patients with paternally inherited 15q11.2-q13 duplications linked to MKRN3 overexpression, presenting with delayed puberty and varying degrees of hypogonadism.
