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Updated: Mar 29, 2026

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
Gershoni-Baruch syndrome: First report of a surviving child
Laura Valfrè1, Anwar Baban2, Maria Cristina Digilio3
1Department of Medical and Surgical Neonatology, Bambino Gesù Children Hospital, Rome, Italy.
Abstract:
Gershoni-Baruch syndrome is an extremely rare malformation complex characterized by omphalocele, diaphragmatic hernia, radial ray defects, and cardiovascular abnormalities. Autosomal recessive inheritance was suggested. To date, academic literature described only seven patients fulfilling the diagnostic criteria for the condition. None survived the neonatal period. This study reports the first individual with Gershoni-Baruch syndrome surviving past early infancy.
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