Evidence map›Paper›PMID 39696567›Full record

ArticleJournal of health, population, and nutrition2024

Burden of neurodevelopmental disorder in Lakki Marwat population of Khyber Pakhtunkhwa, Pakistan.

Muhammad Sheraz, Maria Iqbal, Sumaiya Khan, Sabeena Majeed, Zahid Hameed, Ikram Ullah Khan, Sami Ullah, Amjad Khan

Abstract read
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Article in Journal of health, population, and nutrition, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Muhammad SherazFaculty of Science, Department of Zoology, University of Lakki Marwat, Lakki Marwat, 28420, Khyber Pakhtunkhwa, Pakistan.
Maria IqbalFaculty of Science, Department of Zoology, University of Lakki Marwat, Lakki Marwat, 28420, Khyber Pakhtunkhwa, Pakistan.
Sumaiya KhanFaculty of Science, Department of Zoology, University of Lakki Marwat, Lakki Marwat, 28420, Khyber Pakhtunkhwa, Pakistan.
Sabeena MajeedInstitute of Biological Sciences, Gomal University, Dera Ismail Khan, Pakistan.
Zahid HameedFaculty of Science, Department of Zoology, University of Lakki Marwat, Lakki Marwat, 28420, Khyber Pakhtunkhwa, Pakistan.
Ikram Ullah KhanFaculty of Science, Department of Zoology, University of Lakki Marwat, Lakki Marwat, 28420, Khyber Pakhtunkhwa, Pakistan.
Sami UllahFaculty of Science, Department of Zoology, University of Lakki Marwat, Lakki Marwat, 28420, Khyber Pakhtunkhwa, Pakistan.
Amjad KhanFaculty of Science, Department of Zoology, University of Lakki Marwat, Lakki Marwat, 28420, Khyber Pakhtunkhwa, Pakistan. amjadkhanqau123@hotmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPakistan is a multi-cultural country with different ethnic groups living in both rural and urban communities. There is a significant occurrence of congenital and hereditary neurodevelopmental disorder (NDD) contributing to mortality and morbidity rates.

objectivesThis study aims to explore the prevalence, patterns, and phenotypic spectrum of NDD in district Lakki Marwat population of Khyber Pakhtunkhwa, Pakistan. METHODOLOGY: From 2022 to 2023, a cross-sectional study was conducted and subjects or families with NDD were recruited from district hospitals, rural and urban areas. Door to door survey was also carried out to collect appropriate data. The study gathered phenotypic and descriptive data, clinical information including age, gender, family history, consanguinity and bio-demographic features were recorded.

resultsA total of 276 independent cases/families with NDD were ascertained. The malformations were grouped into major and minor categories. Most of the case/families (58.69%) were sporadic, and 38.04% of the population was classified as having a low-income status. The most frequent family type was a single spouse with children (27.89%), while extended families made up 21.37% of all cases. Demographic variables such as parental consanguinity, syndromic/non-syndromic, familial/sporadic nature, economics status, age of disease onset and pedigree structures showed conspicuous heterogeneity among the major and minor categories of NDD.

conclusionThe high incidence of NDD indicates that nongenetic factors may play a vital role in their etiology which could be diminished by improving the healthcare system.

Indexed as

ConsanguinityNeurodevelopmental DisordersAdolescentAdultChildChild, PreschoolCost of IllnessCross-Sectional StudiesFemaleHumansInfantMalePakistanPrevalenceRural PopulationUrban PopulationConsanguinityGenetic disordersLakki MarwatNeurological disorders

Identifiers

PMID39696567
PMCPMC11656710

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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.