Serum Bone Alkaline Phosphatase and Growth Hormone Levels May Help as a Diagnostic Criteria for Children with Amelogenesis Imperfecta

Journal Title: The Journal of Pediatric Research - Year 2020, Vol 7, Issue 2

Abstract

Aim: The Amelogenesis Imperfecta (AI) term includes numerous inherited congenital enamel defects indicating clinical and genetic heterogeneity. The aim of the present study was to emphasize the importance of the potential prediction of AI via biochemical parameters. Materials and Methods: In total, 50 children were assessed in the study. The subjects included 13 syndromic AI, 22 isolated AI and 15 healthy children with a mean-age of 12.01±3.79 years old. The bone alkaline Phosphatase (BALP) and growth hormone (GH) blood levels of the children were evaluated. All data were statistically analysed by the SPSS 15.0 programme, one-way ANOVA and chi-square tests. Results: 72.7% of syndromic AI and 47.6% of isolated AI group children have higher than normal BALP levels; 33% of syndromic AI and 28% of isolated AI group children have lower than normal blood GH levels. Subjects with AI have statistically significant abnormal blood BALP and GH levels and the presence of an Additional syndrome other than AI did not affect the results. Conclusion: Pediatricians may have a key role in early AI diagnosis via the evaluation of abnormal BALP and GH levels in blood tests and may help in providing comprehensive dental treatment in terms of prevention, prognosis and restoration of teeth in children with AI.

Authors and Affiliations

Didem Öner Özdaş, Sevgi Zorlu, Gamze Aren

Keywords

Related Articles

Demographic, Epidemiologic and Clinical Analyses of Paediatric Patients Hospitalized with Henoch-Schonlein Purpura: A Retrospective Study

Aim: Henoch-Schönlein purpura (HSP) is the most common systemic vasculitis in children. The purpose of this study was to assess the clinical, epidemiological, and laboratory features of 117 children diagnosed with HSP....

Investigations of Microtubule-associated Protein 2 Gene Expression in Spinal Muscular Atrophy

Aim: Spinal muscular atrophy (SMA) is a devastating genetic disease in childhood andff is caused by the absence of functional survival motor neuron (SMN) protein, which leads to impairments of the cytoskeleton, especiall...

A Turkish Version of Children’s Emotional Manifestation Scale: Reliability and Validity Assessment

Aim: This study aims to determine the reliability and validity of the Turkish version of the Children’s Emotional Manifestation scale (T-CEMS). Materials and Methods: The sample of this methodological-type study consist...

Psychometric Properties of a Turkish Version of the Nomophobia Scale for the Nine-Eighteen Age Group

Aim: As a situational phobia, nomophobia is the fear experienced in the absence of a cell phone. Nomophobia leads to situations that negatively affect children’s health. The aim of this study is to conduct validity and r...

Ultrasonographic Screening and the Determination of Risk Factors involved in Developmental Dysplasia of the Hip

Aim: Developmental dysplasia of the hip is an orthopedic problem which is a spectrum of disorders from the instability of the hip joint to total dislocation. Developmental dysplasia of the hip is frequently seen and has...

Download PDF file
  • EP ID EP685481
  • DOI 10.4274/jpr.galenos.2019.60362
  • Views 169
  • Downloads 0

How To Cite

Didem Öner Özdaş, Sevgi Zorlu, Gamze Aren (2020). Serum Bone Alkaline Phosphatase and Growth Hormone Levels May Help as a Diagnostic Criteria for Children with Amelogenesis Imperfecta. The Journal of Pediatric Research, 7(2), -. https://www.europub.co.uk/articles/-A-685481