ARGOMENTIARGOMENTI

Clin Cases Miner Bone Metab. . 9(3): 195–197. doi: PMID: 23289038

Child abuse and osteogenesis imperfecta: how can they be still misdiagnosed? A case report

Abstract

Osteogenesis imperfecta (OI) is a rare hereditary disease caused by mutations in genes coding for type I collagen, resulting in bone fragility. In literature are described forms lethal in perinatal period, forms which are moderate and slight forms where the only sign of disease is osteopenia. Child abuse is an important social and medical problem. Fractures are the second most common presentation after skin lesions and may present specific patterns. The differential diagnosis between slight-moderate forms of OI and child abuse could be very challenging especially when other signs typical of abuse are absent, since both could present with multiple fractures without reasonable explanations. We report a 20 months-old female with a history of 4 fractures occurred between the age of three and eighteen months, brought to authorities’ attention as a suspected child abuse. However when she came to our department physical exa
mination, biochemical tests, total body X-ray and a molecular analysis of DNA led the diagnosis of OI. Thus, a treatment with bisphosphonate and a physical rehabilitation process, according to Vojta method, were started with improvement in bony mineralization, gross motor skills and absence of new fracture. In conclusion our case demonstrates how in any child presenting fractures efforts should be made to consider, besides child abuse, all the other hypothesis even the rarest as OI.

KEYWORDS:

DOI: PMID: 23289038

ID: 1822469

Copyright © 2004 - Tuttosteopatia.it Tutti i diritti riservati
Power by Eter s.r.l. unipersonale P.I. 07180680725
Tuttosteopatia, testata giornalistica reg. n. 10/12 – Registro dei giornali e periodici - Tribunale di Trani del 30 maggio 2012