What is Joubert Syndrome?

Joubert syndrome is an autosomal recessive neurodevelopmental disorder, characterized by a brain abnormality called the “molar tooth sign” which is visible on brain imaging studies (for example, magnetic resonance imaging – MRI). This sign results from the abnormal development of regions in the cerebellar vermis and the brainstem. These specific brain abnormalities resemble the cross-section of a molar tooth when seen on an MRI, hence the name.

The cerebellar vermis is responsible for control of posture and muscles, as well as the movements of the head and eye. The brainstem supervises vital functions such as breathing, pulsations of the heart and temperature control. Therefore abnormal development or absence of those two structures inevitably affects their functions.

Joubert syndrome is estimated to affect between 1 in 80,000 and 1 in 100,000 newborns, but this could be an underestimate given the broad spectrum of features – namely in those with milder manifestations. Although clinical course of the disease can be variable, a majority of affected children survive infancy to reach adulthood.

Clinical presentation

Most individuals with Joubert syndrome present with hypotonia (decreased muscle tone) in infancy, which progresses to ataxia (lack of muscle control during voluntary movements) in early childhood. Ocular, oral-motor and speech dyspraxia (disorder in motor skill development) is also often present, thus hampering the communication abilities.

Respiratory abnormalities are represented by short interchanging episodes of apnea and tachypnea, or episodic tachypnea alone. They tend to occur shortly after birth, escalate with emotional stress and continuously improve with age, generally disappearing around the sixth month of life.

The presence of nystagmus (repetitive, uncontrolled movements of the eye), saccades instead of smooth pursuit and following targets with head movements rather than eye movements are the predominant clinical signs of eye abnormalities in this disease.

While most reports indicate that patients with Joubert syndrome have significant intellectual disability and delayed development, the range of cognitive functions is quite broad. Although some consider that patients with this disease are autistic, many of them are quite interested in social interaction, readily engage in pretend play and exhibit theory of mind – which are all signs inconsistent with autism.

Distinctive facial features characteristic of Joubert syndrome include broad forehead, arched eyebrows, eyelid ptosis, widely spaced eyes, triangle-shaped open mouth configuration and hypotonia of the face. Some individuals with this syndrome also present with polydactyly (extra fingers or toes) of the hands or feet, which can take many forms.

Joubert syndrome can encompass a wide range of additional clinical signs and symptoms, therefore the term “Joubert syndrome and related disorders” has been adopted to describe all disorders presenting with the “molar tooth sign” on brain imaging. Some of the additional features can be kidney disease, liver disease, hormonal problems, retinal dystrophy, ocular colobomas, Hirschsprung's disease and a myriad of other pathologies.

Management of the condition and prognosis

Treatment for Joubert syndrome is mainly symptomatic and supportive, and must be individualized for each child’s unique needs. Infant stimulation with physical, occupational and speech therapy may prove beneficial and help the children achieve their maximum potential. Infants with respiratory abnormalities should be closely monitored. Screening for progressive liver, kidney or eye complications associated with Joubert syndrome-related disorders should be performed on a regular basis.

The prognosis for infants with this syndrome depends on whether or not the cerebellar vermis is partially developed or completely absent, as well as on the severity of other organ involvement. Some children can present with a mild form of the disorder, with good mental development and minimal motor disability, while others may have significant cognitive impairment, drastic lack of muscle control and multi-organ pathology.

There is a rapid progress of research in the field of genetics, so mutations in genes responsible for the disease are increasingly being recognized. This already enables earlier and more accurate prenatal testing and could lead to the replacement of the faulty gene in the future.

While treating neurological disorder is an extremely daunting task due to the complexity of the brain, there is a lot of progress in the development of educational and therapy strategies. High-throughput technologies combined with genetic approaches to evaluate protein-protein interaction will yield a more accurate view of complex mechanism underlying Joubert syndrome.

Further Reading

• All Joubert Syndrome Content
• Joubert Syndrome Genetics

Written by

Dr. Tomislav Meštrović

Dr. Tomislav Meštrović is a medical doctor (MD) with a Ph.D. in biomedical and health sciences, specialist in the field of clinical microbiology, and an Assistant Professor at Croatia's youngest university – University North. In addition to his interest in clinical, research and lecturing activities, his immense passion for medical writing and scientific communication goes back to his student days. He enjoys contributing back to the community. In his spare time, Tomislav is a movie buff and an avid traveler.