Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Burden of Congenital and Hereditary Anomalies in Hazara Population of Khyber Pakhtunkhwa, Pakistan

30 Apr 2022

Abstract excerpt

Background and Objectives: In Pakistan, there is high incidence of congenital and hereditary anomalies (CA) which are a leading cause of infant mortality and morbidity. In order to elucidate the burden and biodemographic correlates of CA, this study was aimed to report the prevalence-pattern and phenotypic attributes of CA in the Hazara population of Khyber Pakhtunkhwa, Pakistan. Methods: In a retrospective...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Congenital limb and hand anomalies
Share to Folate and B Vitamins Research
Share to Genomics and Rare Diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 35799759
DOI: 10.12669/pjms.38.5.5486

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 9 closest

Burden of Congenital and Hereditary Anomalies in Hazara Population of Khyber Pakhtunkhwa, PakistanPMID 35799759Read ↗

Genetic neglect and health inequity: the overlooked burden of alport syndrome in pakistanSemantic proximity Read ↗

Congenital anomalies in children with pre‐ or perinatally acquired cerebral palsy: an international data linkage studySemantic proximity Read ↗

Incidence and prevalence of congenital clubfoot in Apulia: a regional model for future prospective national studiesSemantic proximity Read ↗

Novel VPS13B Mutations in Three Large Pakistani Cohen Syndrome Families Suggests a Baloch Variant with Autistic-Like Features.Semantic proximity Read ↗

Prevalence And Spectrum of Congenital Heart Disease in Nepal: A Systematic Review and Meta-AnalysisSemantic proximity Read ↗

Prevalence of congenital limb defects: Data from birth defects registries in three provinces in Southern Thailand.Semantic proximity Read ↗

Congenital anomalies in children with cerebral palsy: a population‐based record linkage studySemantic proximity Read ↗

Novel Pathogenic Mutation Mapping of ASPM Gene in Consanguineous Pakistani Families with Primary Microcephaly.Semantic proximity Read ↗

The Birth Prevalence of PKU in Populations of European, South Asian and Sub‐Saharan African Ancestry Living in South East EnglandSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.