Anthropometric finding in Nigerian children with sickle cell disease

Folakemi A Oredugba1, Kofo O Savage

  • 1Department of Child Dental Health, College of Medicine, University of Lagos, Nigeria. tored@nova.net.ng

Pediatric Dentistry
|September 6, 2002
PubMed

Insights

Sickle cell disease (SCD) patients show higher rates of maxillary protrusion and Class II malocclusion. While overall height and weight were similar, SCD subjects weighed less at 18 years old.

Area of Science:

  • Medical Science
  • Genetics
  • Pediatrics

Background:

  • Sickle cell disease (SCD) is associated with anthropometric deficits like malocclusion and stunting.
  • Previous reports suggest variations in physical development among SCD patients.

Purpose of the Study:

  • To investigate the prevalence of anthropometric deficits in children with sickle cell disease in Lagos.
  • To compare facial profile and occlusion between SCD subjects and unaffected controls.

Main Methods:

  • A cross-sectional study involving 177 SCD subjects (ages 1-18) and 122 controls.
  • Measurements included facial profile, occlusion, height, weight, and head and mid-upper arm circumference.
  • Data collected from outpatient SCD units and well-baby/surgical emergency clinics.

Main Results:

  • SCD subjects exhibited a higher prevalence of prognathic maxillary profile (21% vs 4%) and Class II malocclusion (21% vs 2%).
  • No significant differences in overall mean height, weight, or head circumference between groups.
  • SCD subjects at 18 years weighed significantly less than controls, and controls had higher MUA circumference.

Conclusions:

  • Sickle cell disease is linked to increased maxillary protrusion and Class II malocclusion.
  • Height and weight differences were minimal, except for lower weight in 18-year-old SCD subjects.
  • Anthropometric variations in SCD patients warrant further investigation.
Abstract