Clinical Signs and Symptoms
ORPHA:1310 Caffey disease
The phenotypic description of this disease is based on an analysis of the biomedical literature and uses the terms of the Human Phenotype Ontology (HPO). Phenotypic abnormalities are presented by order of frequency of occurrence in the patient population, then by alphabetical order inside each frequency group.
- Cellulitis HP:0100658
- Cortical irregularity HP:0005731
Very frequent
- Behavioral abnormality HP:0000708
- Fever HP:0001945
- Hyperesthesia HP:0100963
- Periosteal thickening of long tubular bones HP:0006465
Frequent
- Calvarial hyperostosis HP:0004490
- Cortical thickening of long bone diaphyses HP:0005791
- Facial asymmetry HP:0000324
- Feeding difficulties in infancy HP:0008872
- Increased antibody level in blood HP:0010702
- Proptosis HP:0000520
- Respiratory insufficiency HP:0002093
- Scoliosis HP:0002650
Occasional
Additional information
Further information
Specialised Social Services
Warning
The information provided is based on published scientific articles.
The information provided is estimated for the entire population of patients in routine care. Some phenotypic abnormalities reported here may occur individually with a variable temporality or severity, while others, not listed, may still be encountered. Phenotypic annotations are not yet available for all rare diseases; the annotation process is ongoing.
The information contained in Orphanet is regularly updated. It is possible that discoveries have been made since the last update and have not yet been incorporated.
Professionals are encouraged to always consult the latest scientific publications before making a decision based on the information provided. The information contained in Orphanet is not intended to replace the services of a healthcare professional. Orphanet cannot be held responsible for the deleterious, truncated or erroneous use of any information found in the Orphanet database.