Evidence map›Paper›PMID 40813926›Full record

Observational studyEuropean journal of pediatrics2025

Neurodevelopmental assessment of early treated children with phenylketonuria: insights from Griffith III scales.

Zahraa Abdelmoneim, Heba Eltaher, Mohamed Abdelghafar Hussein, Menna E Hashish

Abstract readObservational Study
In one paragraph

Observational study 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.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Zahraa AbdelmoneimDepartement of Pediatrics, Genetics and Metabolic Unit, Faculty of Medicine, Mansoura University, Mansoura, Egypt. hzahraa211@gmail.com.ORCID http://orcid.org/0009-0005-3632-6410
Heba EltaherDepartement of Pediatrics, Genetics and Metabolic Unit, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Mohamed Abdelghafar HusseinDepartment of Pediatrics, Faculty of Medicine, Kafrelsheikh University, Kafrelsheikh, Egypt.
Menna E HashishDepartment of Pediatrics, Faculty of Medicine, Mansoura University, Mansoura, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neonatal screening of phenylketonuria (PKU) and early treatment are fundamental to prevent mental retardation in children. Unfortunately, it has been observed that some neurological sequelae may still be exhibited despite these preventive strategies. Assessment of the neurodevelopment of early treated children may aid in understanding the devastating effect of PKU on the developing brain, so this study aimed to investigate the neurodevelopmental outcome of early-treated children with PKU using Griffiths-III developmental scales. We conducted an observational single-center case-control study on a total of 60 children.  We compared the neurodevelopmental profile of two groups of children (PKU group = 30 and healthy control group = 30) using Griffiths-III developmental scales. Also PKU children were divided into two subgroups according to their phenylalanine level: controlled and uncontrolled. There were significant decreases in the mean of developmental quotients (DQs) of Griffiths-III subscales A, B, C, D, and general development of PKU group. While there was insignificant difference in the DQ of subscale E (gross motor) among the two groups, there was a significant difference between the two PKU subgroups regarding the developmental quotient of subscales A, B, C, E, and general development. Also, there was a statistically significant correlation between phenylalanine (Phe) levels and the mean of DQs of all Griffiths-III subscales.

conclusionEarly- treated PKU children are at risk of poor neurodevelopmental outcome even if their gross motor function is normal and this defect is negatively correlated with phenylalanine levels. WHAT IS KNOWN: • PKU is an inborn error of metabolism that causes mental retardation if not treated early. • Neonatal screening and early treatment prevent mental retardation. WHAT IS NEW: • Despite neonatal screening and early treatment, PKU children still exhibit mental function impairment. • The Griffiths III developmental scales is the first time to be used to assess mental functions in PKU children.

Indexed as

Child DevelopmentDevelopmental DisabilitiesNeurodevelopmental DisordersPhenylketonuriasCase-Control StudiesChildChild, PreschoolFemaleHumansInfantInfant, NewbornMaleNeonatal ScreeningPhenylalaninePhenylalanineGriffiths III developmental scalesNeurodevelopmental profilePhenylketonuria

Identifiers

PMID40813926
PMCPMC12354494

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.