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

Early Diagnosis of Classic Homocystinuria in Kuwait through Newborn Screening: A 6-Year Experience

17 Aug 2021

Abstract excerpt

Kuwait is a small Arabian Gulf country with a high rate of consanguinity and where a national newborn screening program was expanded in October 2014 to include a wide range of endocrine and metabolic disorders. A retrospective study conducted between January 2015 and December 2020 revealed a total of 304,086 newborns have been screened in Kuwait. Six newborns were diagnosed with classic homocystinuria with an...

Read the complete abstract on PubMed

Topics

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

Share to Folate and B Vitamins Research
Share to Metabolism and Genetic Disorders
Share to Neonatal Health and Biochemistry

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 34449519
DOI: 10.3390/ijns7030056

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 · 12 closest

Early Diagnosis of Classic Homocystinuria in Kuwait through Newborn Screening: A 6-Year ExperiencePMID 34449519Read ↗

Enzymatic Testing for Mucopolysaccharidosis Type I in Kuwaiti Newborns: A Pilot Study Toward Newborn ScreeningSemantic proximity Read ↗

The Spectrum of Mutations of Homocystinuria in the MENA Region.Semantic proximity Read ↗

An Assessment of Traditional and Genomic Screening in Newborns and their Applicability for AfricaSemantic proximity Read ↗

Newborn Screening for Hereditary Tyrosinemia Type I in Québec: Update.Semantic proximity Read ↗

Combined Newborn Screening Allows Comprehensive Identification also of Attenuated Phenotypes for Methylmalonic Acidurias and Homocystinuria.Semantic proximity Read ↗

Mutations of a country: a mutation review of single gene disorders in the United Arab Emirates (UAE).Semantic proximity Read ↗

A universal carrier test for the long tail of Mendelian disease.Semantic proximity Read ↗

Classical homocystinuria: A common inborn error of metabolism? An epidemiological study based on genetic databasesSemantic proximity Read ↗

Combined genetic screening and traditional newborn screening to improve the screening efficiency of congenital hypothyroidismSemantic proximity Read ↗

An early onset form of methylenetetrahydrofolate reductase deficiency: a report of a family from Kuwait.Semantic proximity Read ↗

Screening of hereditary elliptocytosis caused by SPTB mutations and identification of its association with significant jaundice among Thai neonates.Semantic proximity Read ↗

[Newborn screening and variant analysis for methionine adenosyltransferase I/III deficiency].Semantic proximity Read ↗

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