Preterm infant with diprosopus and holoprosencephaly

Preterm infant with diprosopus and holoprosencephaly

Diprosopus is an extremely rare congenital anomaly involving craniofacial duplication. The etiology and pathophysiology remain unknown, and no genetic mutations have been definitively associated with the condition. This case describes an infant born at 27-weeks completed gestation with multiple cong...

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Veröffentlicht in:Clinical case reports 2021, Vol.9 (12), p.e05163-e05163
Hauptverfasser: Nair, Nitya M, Swarr, Daniel T, Barnes-Davis, Maria E
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Sprache:eng
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container_title Clinical case reports
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creator Nair, Nitya M
Swarr, Daniel T
Barnes-Davis, Maria E
description Diprosopus is an extremely rare congenital anomaly involving craniofacial duplication. The etiology and pathophysiology remain unknown, and no genetic mutations have been definitively associated with the condition. This case describes an infant born at 27-weeks completed gestation with multiple congenital anomalies including diprosopus and discusses the implications of prenatal diagnosis.
doi_str_mv 10.1002/ccr3.5163
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source Wiley Online Library Open Access; DOAJ Directory of Open Access Journals; Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
title Preterm infant with diprosopus and holoprosencephaly
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