Oral and radiographic features of Majewski osteodysplastic dwarfism: a case report

Authors

  • Ntaoleng J Mohapi University of Witwatersrand
  • Mzubanzi Mabongo University of Pretoria

DOI:

https://doi.org/10.54450/saradio.2022.60.1.641

Keywords:

autosomal, panorex, microdontia, small roots

Abstract

Majewski osteodyplastic primordial dwarfism type II (MOPD II) is a rare, autosomal recessive disorder characterised by severe intrauterine and postnatal growth retardation. A case report with a distinct rare oral and radiographic feature with MOPD II is presented. It differs from the description of primordial dwarfism with characteristics of small head diameter at birth, which progresses to severe microcephaly and mild mental retardation. 

Author Biographies

Ntaoleng J Mohapi, University of Witwatersrand

Wits Oral Health Centre, School of Oral Health Sciences, University of Witwatersrand

Radiographer and Lecturer

Mzubanzi Mabongo, University of Pretoria

School of Dentistry, Department of Maxillo-Facial and Oral Surgery, University of Pretoria

Head of Department

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Published

2022-05-31

Issue

Section

Case Reports