hrp0094p2-333 | Multisystem endocrine disorders | ESPE2021

An Early Diagnosis of Prohormone Convertase Deficiency

Elmaoğulları Selin , Keskin Meliksah , Savaş Erdeve Şenay , Arifoğlu Barış İlter , Kılıc Mustafa , Ozbay Hoşnut Ferda , Melek Boynukalın Melahat , Cetinkaya Semra ,

Introduction: Prohormone convertases are a family of proteins that mediate the processing and activation of peptide hormones and neuropeptide precursors. Homozygous mutations of the PCSK1 gene result in prohormone convertase 1 deficiency that is characterized by diarrhea, hypoglycemia, multiple pituitary hormone deficiency beginning from neonatal period and obesity beginning after infancy.Case: A 35-day-old boy was referred to our hospit...