INFANTILE CORTICAL HYPEROSTOSIS
Infantile cortical hyperostosis or Caffey disease is a rare genetic disorder caused by a mutation in the collagen 1 gene. The mechanism of the disease has not yet been fully elucidated, but the most important factor in the pathogenesis and the consequence of the mutation is periosteal inflammation. T...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | Slovenian |
| Published: |
The Society for Children with Metabolic Disorders
2021-06-01
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| Series: | Slovenska pediatrija |
| Subjects: | |
| Online Access: |
http://www.slovenskapediatrija.si/Portals/0/Clanki/2021/Slovpediatr-2021-2-06en.pdf
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