# More Than Just a Floppy Baby: Maintaining High Clinical Suspicion of Infant Botulism

**Authors:** Natalee Sarintra, Rachel Ekdahl, Sara C Sanders, Brittany Slagle, Katherine Tang

PMC · DOI: 10.7759/cureus.102021 · 2026-01-21

## TL;DR

A four-week-old baby in Arkansas was diagnosed with infant botulism after showing symptoms like lethargy and feeding difficulties, highlighting the importance of early suspicion and detailed exposure history for timely treatment.

## Contribution

This case highlights the diagnostic challenges of infant botulism and emphasizes the importance of early clinical suspicion and thorough exposure history.

## Key findings

- The patient's symptoms initially mimicked a viral illness but were later attributed to botulinum toxin type B.
- Administration of botulinum immune globulin led to gradual clinical improvement.
- The case underscores the need for high clinical suspicion and detailed exposure history to avoid misdiagnosis.

## Abstract

Infant botulism is a rare and life-threatening condition if left untreated. We report the case of a previously healthy four-week-old male in Arkansas, who presented with progressive lethargy, feeding difficulties, and respiratory compromise following a recent viral respiratory illness. His clinical course was notable for worsening hypotonia, absent reflexes, and eventual respiratory failure requiring intubation. Extensive evaluation for infectious, neurologic, and metabolic causes was initially unrevealing, but further exposure history revealed constipation paired with recent soil exposure, raising suspicion for infant botulism. Botulinum immune globulin (BabyBIG®) was administered, with subsequent gradual clinical improvement. Stool testing later confirmed the presence of botulinum toxin type B. The patient was discharged in stable condition, tolerating full oral feeds, and without further complications. This case underscores the diagnostic difficulty of infant botulism due to early age at presentation, anchoring bias with diagnosis of a recent viral illness, and overlapping symptoms with other neonatal conditions. A detailed exposure history is critical, and early clinical suspicion can facilitate timely treatment and improve outcomes.

## Linked entities

- **Diseases:** infant botulism (MONDO:0015804)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Diseases:** respiratory compromise (MESH:D012131), diarrhea (MESH:D003967), fatigue (MESH:D005221), respiratory distress (MESH:D012128), fever (MESH:D005334), neurologic decline (MESH:D009461), vomiting (MESH:D014839), respiratory muscle paralysis (MESH:D012133), cranial nerve palsies (MESH:D003389), inflammatory (MESH:D007249), Rhinovirus/Enterovirus infection (MESH:D004769), neurodegenerative (MESH:D019636), traumatic injuries (MESH:D014947), respiratory illness (MESH:D012140), head trauma (MESH:D006259), oral motor weakness (MESH:D018908), meningitis (MESH:D008580), SMA (MESH:D009134), neonatal and infant disorders (MESH:D007232), Botulism (MESH:D001906), inborn errors of metabolism (MESH:D008661), constipation (MESH:D003248), neuromuscular weakness (MESH:D009468), muscular dystrophies (MESH:D009136), ID (MESH:D003141), neuromuscular blockade (MESH:D020879), sepsis (MESH:D018805), lethargic (MESH:D004674), epilepsy (MESH:D004827), hypotonia (MESH:D009123), neurologic, metabolic, (MESH:D001928), death (MESH:D003643), intracranial abnormalities (MESH:D001927), nasal congestion (MESH:D009668), congestion (MESH:D002311), encephalitis (MESH:D004660), congenital hypothyroidism (MESH:D003409), infections (MESH:D007239), pleocytosis (MESH:D007964), lethargy (MESH:D053609), dehydration (MESH:D003681)
- **Chemicals:** pyruvate (MESH:D019289), oxygen (MESH:D010100), ammonia (MESH:D000641), lactate (MESH:D019344), ampicillin (MESH:D000667), Botulinum immune globulin (-), T4 (MESH:D013974), amino acids (MESH:D000596), ceftriaxone (MESH:D002443), acylcarnitine (MESH:C116917)
- **Species:** Clostridium botulinum (species) [taxon 1491], Enterovirus (genus) [taxon 12059], Cytomegalovirus (genus) [taxon 10358], human gammaherpesvirus 4 (Epstein Barr virus, no rank) [taxon 10376], Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12923330/full.md

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Source: https://tomesphere.com/paper/PMC12923330