Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add filters








Type of study
Language
Year range
1.
Oman Medical Journal. 2010; 25 (2): 134-136
in English | IMEMR | ID: emr-105299

ABSTRACT

Caffey disease or Infantile Cortical Hyperostosis [ICH] is a rare and mostly self limiting condition affecting young infants. It is characterized by acute inflammation of the periostium and the overlying soft tissue and is accompanied by systemic changes of irritability and fever. Diagnosis may be delayed as this disorder mimics a wide range of diseases including osteomyelitis, hypervitaminosis A, scurvy, bone tumors and child abuse. The emphasis here is to remind clinicians about the existence of the disease in this country


Subject(s)
Humans , Male , Hydrops Fetalis , Gestational Age , Ribs/abnormalities , Infant, Newborn
SELECTION OF CITATIONS
SEARCH DETAIL