Sonographic 'molar tooth' sign in the diagnosis of Joubert syndrome.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 21370303.
- Also identified by DOI 10.1002/uog.8979.
- 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
The characteristic imaging finding common to Joubert syndrome and related disorders is the 'molar tooth' sign. The prenatal diagnosis of Joubert syndrome using both ultrasound and fetal magnetic resonance imaging (MRI) in families with an affected child has been reported previously. We report two cases in which the molar tooth sign was identified by sonography at 26 + 4 weeks and at 20 + 6 weeks, respectively, prior to fetal MRI or genetic testing. In both cases the finding was subsequently confirmed on fetal MRI. As definitive prenatal genetic testing may not be conclusive in Joubert syndrome, the ability to identify the molar tooth sign sonographically before 24 weeks provides a valuable adjunct to prenatal diagnosis.
Medical subject headings
- Abnormalities, Multiple
- Brain
- Cerebellar Diseases
- Echoencephalography
- Eye Abnormalities
- Kidney Diseases, Cystic
- Ultrasonography, Prenatal