@article{ref1,
title="Osteogenesis imperfecta in a Nigerian neonate: a case report",
journal="West African journal of medicine",
year="2008",
author="Oyinloye, O. O.",
volume="27",
number="2",
pages="114-116",
abstract="BACKGROUND: Osteogenesis imperfecta is an inherited disease where the basic pathology is of defective collagen. It is a rare disorder with a reported incidence of 1/25000-1/30000. Four variants are recognized clinically, of which type II is the most severe form. Clinically the hall marks of the disease are multiple fractures and osteopenia. OBJECTIVE: This case is being presented because of its rare incidence, and to highlight the radiological features distinguishing it from battered baby syndrome occurring from child abuse. CASE REPORTS: An eight day old Nigeria neonate, with clinico radiological features highly suggestive of type II osteogenesis imperfecta is presented. CONCLUSION: Emphasis on the radiological features, especially those distinguishing it from battered baby syndrome which has a similar appearance are discussed.<p /><p>Language: en</p>",
language="en",
issn="0189-160X",
doi="",
url="http://dx.doi.org/"
}