Facial dysmorphism: a marker of autosomal dominant cranial diabetes insipidus.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 1920373.
- Also identified by PMC identifier 1016986.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
We report a family with autosomal dominant cranial diabetes insipidus in which a characteristic facial appearance of hypertelorism, broad and prominent nasal bridge, short nose, and long philtrum is seen in affected members.
Medical subject headings
- Diabetes Insipidus
- Facial Bones
- Genes, Dominant
- Skull