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Case Report

Published on 10 May 2023

Case Report: short stature, kidney anomalies, and cerebral aneurysms in a novel homozygous mutation in the PCNT gene associated with microcephalic osteodysplastic primordial dwarfism type II

in Pediatric Endocrinology

  • Maddalena Petraroli
  • Antonio Percesepe
  • Maria Piane
  • Francesca Ormitti
  • Eleonora Castellone
  • Margherita Gnocchi
  • Giulia Messina
  • Luca Bernardi
  • Viviana Dora Patianna
  • Susanna Maria Roberta Esposito
Case Report: short stature, kidney anomalies, and cerebral aneurysms in a novel homozygous mutation in the PCNT gene associated with microcephalic osteodysplastic primordial dwarfism type II
Frontiers in Endocrinology
doi 10.3389/fendo.2023.1018441
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  • 1 citation