Related Articles
Identification of AAAS gene mutation in Allgrove syndrome: A report of three cases
Mild Camurati‑Engelamann disease presenting with exophthalmos as the first and only manifestation: A case report
Distinct magnetic resonance imaging features in a patient with novel RARS2 mutations: A case report and review of the literature
Lifelong deformities in an adult caused by vitamin D‑dependent rickets type 1A: A case report
Neonatal congenital leukemia caused by several missense mutations and AFF1‑KMT2A fusion: A case report