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Updated: Jul 4, 2026

A Common Marmoset Model of Mother-Infant Intervention for Breastfeeding Disorders in the Presence of Paternal Inhibition and Maternal Neglect

A Common Marmoset Model of Mother-Infant Intervention for Breastfeeding Disorders in the Presence of Paternal Inhibition and Maternal Neglect

Published on: September 22, 2023

Severe failure to thrive in infant.

Deepti Allapathi¹, Dora Alvarez, Swati Dave-Sharma

¹Department of Pediatrics, Division of Critical Care, Lincoln Medical and mental health center, Bronx, New York, USA.

Clinical Pediatrics

|June 10, 2008

Summary

This summary is machine-generated.

Failure to thrive in infants can signal serious illness like Bartter syndrome. Early diagnosis via history, exam, and electrolytes is crucial for management and preventing life-threatening outcomes.

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Assessment and Evaluation of the High Risk Neonate: The NICU Network Neurobehavioral Scale

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Published on: August 25, 2014

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Published on: September 22, 2023

Assessment and Evaluation of the High Risk Neonate: The NICU Network Neurobehavioral Scale

Assessment and Evaluation of the High Risk Neonate: The NICU Network Neurobehavioral Scale

Published on: August 25, 2014

Area of Science:

Pediatrics
Nephrology
Genetics

Background:

Failure to thrive (FTT) in infants presents diagnostic challenges, often masking severe underlying conditions.
Bartter syndrome, a rare genetic disorder, is a significant, albeit uncommon, cause of FTT.
Early recognition and management of Bartter syndrome are critical for infant health outcomes.

Observation:

This article details a case of severe FTT in an infant caused by the neonatal form of Bartter syndrome.
The infant presented with characteristic manifestations requiring careful clinical evaluation.
Diagnostic methods included detailed history, physical examination, and electrolyte pattern analysis.

Findings:

Neonatal Bartter syndrome was confirmed as the etiology of severe FTT.
The specific clinical manifestations and electrolyte abnormalities consistent with Bartter syndrome were identified.
Successful management strategies were implemented based on the diagnosis.

Implications:

Highlights the importance of considering rare genetic disorders like Bartter syndrome in cases of unexplained infant FTT.
Emphasizes the critical role of prompt diagnosis and appropriate management in preventing severe complications and improving infant prognosis.
Underscores the need for increased awareness among clinicians regarding the presentation and diagnostic pathway of neonatal Bartter syndrome.