Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Osteopenia and phenylketonuria.

D J Carson1, L G Greeves, L E Sweeney

  • 1Department of Child Health, Queens University, Belfast, Northern Ireland.

Pediatric Radiology
|January 1, 1990
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Association analysis of proopiomelanocortin (POMC) haplotypes in type 1 diabetes in a UK population.

Diabetes & metabolism·2011
Same author

Polymorphisms of the macrophage migration inhibitory factor gene in a UK population with Type 1 diabetes mellitus.

Diabetic medicine : a journal of the British Diabetic Association·2010
Same author

No association between routinely recorded infections in early life and subsequent risk of childhood-onset Type 1 diabetes: a matched case-control study using the UK General Practice Research Database.

Diabetic medicine : a journal of the British Diabetic Association·2008
Same author

Secular trends, disease maps and ecological analyses of the incidence of childhood onset Type 1 diabetes in Northern Ireland, 1989-2003.

Diabetic medicine : a journal of the British Diabetic Association·2007
Same author

The PAX4 gene variant A1168C is not associated with early onset Type 1 diabetes in a UK population.

Diabetic medicine : a journal of the British Diabetic Association·2006
Same author

Higher incidence of childhood-onset type 1 diabetes mellitus in remote areas: a UK regional small-area analysis.

Diabetologia·2006
Same journal

The invisible footprint: why planetary health is a pediatric radiologist's obligation.

Pediatric radiology·2026
Same journal

The radiographic bubbly fecal pattern of intestinal pneumatosis in newborns revisited.

Pediatric radiology·2026
Same journal

Regional differences in fetal fat accretion in small-for-gestational-age fetuses assessed by quantitative magnetic resonance imaging.

Pediatric radiology·2026
Same journal

Thermal ablation of lung metastases in children: what every paediatric radiologist should know.

Pediatric radiology·2026
Same journal

Prediction of early recurrence in primary intussusception: development of an ultrasound-based radiomics and deep learning nomogram.

Pediatric radiology·2026
Same journal

Pediatric SARS-CoV-2 long term outcomes study: chest radiographic and computed tomography findings at baseline.

Pediatric radiology·2026
See all related articles

Young adults with phenylketonuria (PKU) on a restricted diet show reduced bone mineral content. Further studies in children are needed to ensure optimal bone health in adulthood.

Area of Science:

  • Biochemistry
  • Orthopedics
  • Pediatrics

Background:

  • Phenylketonuria (PKU) is an inherited metabolic disorder requiring lifelong dietary management.
  • Dietary treatment for PKU involves restricting natural protein and supplementing with amino acids, minerals, and vitamins.
  • Bone health is a potential concern in individuals with PKU due to metabolic alterations.

Purpose of the Study:

  • To assess trabecular bone mineral content in young adults with phenylketonuria.
  • To compare bone mineral density in treated PKU patients with a normal population.
  • To identify potential long-term effects of PKU treatment on skeletal health.

Main Methods:

  • Quantitative computed tomography (QCT) was used to measure bone mineral content.
  • Eleven young adults diagnosed with phenylketonuria and treated since early childhood participated.

Related Experiment Videos

  • Bone mineral content was compared between the PKU group and a healthy control group.
  • Main Results:

    • A significant reduction in trabecular bone mineral content was observed in patients with phenylketonuria.
    • The bone mineral content in PKU patients was lower compared to the normal population.
    • These findings suggest a potential impact of PKU and its management on bone health.

    Conclusions:

    • Individuals with phenylketonuria treated from early childhood may experience reduced bone mineral content in adulthood.
    • Longitudinal studies in younger PKU patients are recommended to optimize bone mineralization strategies.
    • Ensuring adequate bone mineralisation throughout development is crucial for long-term skeletal integrity in PKU.