Joubert syndrome and related disorders
MONDO:0015369Also known as: JSRD, Joubert syndrome and related disorders
- MONDO:
- MONDO:0015369
- Orphanet:
- 140874 ↗
Rare disease35 associated genes
Description
Joubert syndrome (JS) and related disorders (JSRD) are a group of developmental delay/multiple congenital anomaly syndromes in which the mandatory feature is the "molar tooth sign'' (MTS), a complex midbrain-hindbrain malformation recognizable on brain imaging. The MTS is characterized by cerebellar vermis hypodysplasia, thickening and malorientation of the superior cerebellar peduncles and abnormally deep interpeduncular fossa.
Associated genes
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