Prevalence of adrenal 21‐hydroxylase deficiency in neonates born in the West Midlands: a retrospective study

Rudd, B. T.

doi:10.1007/bf01800871

J of Inher Metab Disea

1986

DOI: 10.1007/bf01800871

|View full text |Cite

Prevalence of adrenal 21‐hydroxylase deficiency in neonates born in the West Midlands: a retrospective study

B. T. Rudd

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

Supporting

Mentioning

Contrasting

Year Published

1987

2012

Publication Types

Select...

Article4

Relationship

Self Cite0

Independent4

Authors

Journals

Cited by 4 publications

References 1 publication

(1 reference statement)

Supporting

Mentioning

Contrasting

Order By: Relevance

A systematic review of evidence for the appropriateness of neonatal screening programmes for inborn errors of metabolism

Thomason

Lord

Bain

et al. 1998

Journal of Public Health

View full text Add to dashboard Cite

Large-scale trials of screening for biotinidase, CAH, MCAD and GA1 should be conducted, with careful evaluation to establish their clinical effectiveness and cost-effectiveness in practice. Screening for the latter two disorders would be dependent upon the use of tandem mass spectrometry (tandem MS). The application of tandem MS to newborn screening requires further evaluation. The extension of neonatal screening programmes to other IEMs is not currently justified.

show abstract

A systematic review of evidence for the appropriateness of neonatal screening programmes for inborn errors of metabolism

Thomason

Lord

Bain

et al. 1998

Journal of Public Health

View full text Add to dashboard Cite

show abstract

Should we screen for congenital adrenal hyperplasia? A review of 117 cases.

Virdi¹,

Rayner²,

Rudd³

et al. 1987

Archives of Disease in Childhood

View full text Add to dashboard Cite

SUMMARY A total of 117 patients with congenital adrenal hyperplasia who were under the care of paediatricians at Birmingham Children's Hospital between 1958 and 1985 were reviewed retrospectively. There were 47 boys (40%) and 70 girls (60%); 30 of the 47 boys (64%) and 38 of the girls (58% of the 66 whose salt state was known) were salt losers. In all salt losers the condition was diagnosed before the age of 6 months, 90% of the diagnoses being made during the first month. The ratio of boys to girls, the distributions of salt losers to non-salt losers, and the age at diagnosis were studied in relation to the year of birth. Early diagnosis was found to be more common in children born after 1970 due partly to the introduction of a method of assaying the concentration of 17a-hydroxyprogesterone in serum, partly to an increase in the number of paediatricians in the West Midlands, and partly to the appointment of a peadiatric endocrinologist. A neonatal screening programme does not seem to be necessary.

show abstract

Incidence and clinical features of congenital adrenal hyperplasia in Great Britain

Khalid¹,

Oerton²,

Dezateux³

et al. 2012

Arch Dis Child

View full text Add to dashboard Cite

show abstract

scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.

Contact Info

hi@scite.ai

10624 S. Eastern Ave., Ste. A-614

Henderson, NV 89052, USA

Blog Terms and Conditions API Terms Privacy Policy Contact Cookie Preferences Do Not Sell or Share My Personal Information

Made with 💙 for researchers

Part of the Research Solutions Family.

Prevalence of adrenal 21‐hydroxylase deficiency in neonates born in the West Midlands: a retrospective study

Cited by 4 publications

References 1 publication

A systematic review of evidence for the appropriateness of neonatal screening programmes for inborn errors of metabolism

A systematic review of evidence for the appropriateness of neonatal screening programmes for inborn errors of metabolism

Should we screen for congenital adrenal hyperplasia? A review of 117 cases.

Incidence and clinical features of congenital adrenal hyperplasia in Great Britain

Contact Info

Product

Resources

About