Alum Robinson, Coe Publish Article in Neonatal Care Journal

Alum Robinson, Coe Publish Article in Neonatal Care Journal

<p>Melissa K. Robinson, MSN '19, and Kristi Coe, consulting associate, published "<a href="https://journals.lww.com/advancesinneonatalcare/Abstract/9000/A_Case_Report_of_Donnai_Barrow_Syndrome.99663.aspx">A Case Report of&nbsp;Donnai-Barrow Syndrome</a>" article in the Advances in Neonatal Care with former DUSON&nbsp;assistant professor Wanda Bradshaw.&nbsp;</p>

CoeMelissa K. Robinson, MSN '19, and Kristi Coe, consulting associate, published "A Case Report of Donnai-Barrow Syndrome" article in the Advances in Neonatal Care with former DUSON assistant professor Wanda Bradshaw. 

Abstract

Background

A genetic disorder should be considered when an infant presents with multiple congenital anomalies. Because of the acute presentation of an infant with multiple life-threatening defects, a genetic diagnosis of a rare disorder took weeks to delineate.

Clinical Findings

This case describes a late preterm infant who presented at birth with congenital diaphragmatic hernia, tetralogy of Fallot, cleft lip, low-set ears and hypertelorism.

Primary Diagnosis

Donnai-Barrow syndrome was the final diagnosis confirmed by a defect observed on the LRP2 (2q31.1) gene using sequence analysis. This is a rare disorder that presents with a variety of phenotypic features in infants.

Interventions

Initial neonatal resuscitation in the delivery room included intubation, positive pressure ventilation, and oxygen supplementation. Extracorporeal membrane oxygenation therapy was initiated from day of life 3 to 15. Initial surgery included correction of the congenital diaphragmatic hernia, and further surgical procedures included tracheostomy, gastrostomy tube, circumcision, ventricular septal defect repair, and cleft lip repair. Physical, occupational, and speech therapies were also initiated.

Outcomes

The infant was transported to a pediatric rehabilitation facility at 6 months of life for further management of his chronic lung disease requiring tracheostomy with ventilator dependence.

Practice Recommendations

Early recognition and diagnosis of genetic syndromes can improve family education and guide treatment interventions. An underlying syndrome should be suspected when an infant presents with multiple congenital defects. Infants with Donnai-Barrow syndrome should have thorough cardiac, neurologic, ophthalmologic, audiologic, and renal examinations due to the gene mutation effects on those systems.

 

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