Evidence map›Paper›PMID 41055751›Full record

ArticleEuropean journal of pediatrics2025

Application of the neonatal 'floppy module' to older infants: can it be used for differential diagnosis?

Costanza Cutrona, Martina Sbarbati, Martina Malaspina, Chiara Velli, Francesca Sini, Roberta Onesimo, Giorgia Coratti, Domenico M Romeo, Marika Pane, Eugenio Mercuri

Abstract read
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Article in European journal of pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Costanza CutronaPediatric Neurology, Università Cattolica del Sacro Cuore, Rome, Italy.
Martina SbarbatiPediatric Neurology, Università Cattolica del Sacro Cuore, Rome, Italy.
Martina MalaspinaPediatric Neurology, Università Cattolica del Sacro Cuore, Rome, Italy.
Chiara VelliPediatric Neurology and Psychiatry Unit, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
Francesca SiniPediatric Neurology and Psychiatry Unit, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
Roberta OnesimoPediatric Unit, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
Giorgia CorattiPediatric Neurology, Università Cattolica del Sacro Cuore, Rome, Italy.
Domenico M RomeoPediatric Neurology, Università Cattolica del Sacro Cuore, Rome, Italy.
Marika PanePediatric Neurology, Università Cattolica del Sacro Cuore, Rome, Italy.
Eugenio MercuriPediatric Neurology, Università Cattolica del Sacro Cuore, Rome, Italy. eugeniomaria.mercuri@unicatt.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study we applied the 'floppy module', originally developed for newborns with hypotonia, to older infants in order to establish the range of findings in both low-risk infants and in those with hypotonia due to different etiologies. Data were collected from 413 assessments obtained in 159 low-risk infants assessed at different ages between the age of 3 and 24 months. The distribution of findings in the low-risk infants was similar to the data previously obtained in low-risk newborns, with all assessments having optimal findings (column 3) on all items. The only item with a small number of findings outside column 3 was tendon reflexes. The module was also applied to a cohort of 57 infants with hypotonia older than 3 months in order to identify individual items that may be useful in differential diagnosis. Items assessing antigravity movements were the most sensitive to identify neuromuscular disorders. Dysmorphic features and other organ involvement were most suggestive of genetic disorder, while seizures were a reliable indicator of CNS involvement.

conclusionOur findings suggest that the neonatal floppy module can be reliably administered also in infants from the age of 3 months. The pilot application of the module in infants with hypotonia from the age of 3 months also suggested that the module could be used to help the clinician in the differential diagnosis of infants with hypotonia. WHAT IS KNOWN: • Hypotonia is a relatively common finding in the neonatal period and can be due to multiple causes. • As hypotonia can be observed also after the neonatal period and clinicians often face the challenge of differential diagnosis, the question has arisen whether the 'floppy module' validated in newborns could also be used in infants. WHAT IS NEW: • Most of the infants with hypotonia, between the age of 3 to 24 months, have a diagnosis of neuromuscular disorders. • Most of the infants with CNS involvement and with genetic diagnosis, who may have shown hypotonia in the neonatal period, by 6 to 12 months have normal or increased tone.

Indexed as

Muscle HypotoniaNeuromuscular DiseasesChild, PreschoolDiagnosis, DifferentialFemaleHumansInfantInfant, NewbornMalePilot ProjectsFloppy infant moduleHypotoniaNeonatal neurological examinationNeuromuscular disorders

Identifiers

PMID41055751
PMCPMC12504406

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