craniosynostosis with anomalies of the cranial base and digits
MONDO:0009037
Outbreak surveillance
Global reported eventsExplore recent public health notices potentially related to craniosynostosis with anomalies of the cranial base and digits. Results are keyword matches, not yet verified disease-to-outbreak relationships.
View craniosynostosis with anomalies of the cranial base and digits on the outbreak map →Craniosynostosis with anomalies of the cranial base and digits
Craniosynostosis with anomalies of the cranial base and digits is a syndrome characterized by atypical development in a fetus's limbs and skull. People with this condition are often missing the middle parts of the second and fifth fingers, as well as their thumbs, though the thumbs may be improperly positioned. The big toes may also be missing or improperly positioned. Additionally, the bones in the skull close too early in development (craniosynostosis), and bones at the skull base grow incorrectly. Woon et al. first reported the condition in 1980 in a pair of male twins of Mexican American and Sioux Indian ancestry with no chromosomal abnormalities. Both died within 3 months of birth.
Background only. Canonical identity remains MONDO; clinical-trial relationships come from ClinicalTrials.gov.Drugs being studied
Disease identity and terminology: MONDO. Trial relationships: ClinicalTrials.gov.