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ORPHA:140874· Joubert syndrome and related disorders

Визначення(English summary)

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.

Поширеність
1-9 / 100 000
Успадкування
Autosomal recessive, X-linked recessive
Вік початку
Infancy, Neonatal