Joubert syndrome
Updates to Article Attributes
Joubert anomaly (also known as vermian aplasia or molar tooth midbrain-hindbrain malformation) is an autosomal recessive disorder where there is a variable degree of cerebellar vermal agenesis.
When associated with anomalies of the kidneys, liver and/or eyes then the term Joubert syndrome and related disorders (JSRD) is used.
Epidemiology
The prevalence of Joubert syndrome is approximately 1 in 100000. There are numerous associations which are variably present 5:
- ocular abnormalities
- coloboma
- retinal dysplasia : 50% - some authors advocate dividing Joubert syndrome patients into two groups according to the presence or absence of retinal dysplasia 5
- nephronopthiasis
- multicystic dysplastic kidneys (MCDK) : 30%
- hepatic fibrosis
- polydactyly : 15%
Clinical presentation
Affected individuals usually present with ataxia and have dysmorphic facies, global developmental delay, hypotonia, rapid breathing and oculomotor apraxia. There is significant range in the degree of cognitive impairment with IQ ranging form 30 to 80, although presence of speech and motor deficits makes assessment difficult 7.
Typically, patients have nystagmus and inability of smooth pursuit of a moving object 5.
Pathology
Joubert syndrome patients are a heterogeneous population in terms of genetics with some having a mutation of chromosome 9q34.3 - many do not 4. At least 10 genes have been implicated, relating to subcellular organelle the primary cilium and basal body; as such JS is one of a number of related disorders known as ciliopathies 7,8.
Radiographic features
Cross-sectional axial imaging demonstrates isolated abnormality of the cerebellum, consisting of:
- small dysplastic or aplastic cerebellar vermis
- absence of fibre decussation in the superior cerebellar peduncles and pyramidal tracts 2
- abnormal inferior olivary nucleus
- dysplasia and heterotopia of cerebellar nuclei
The posterior fossa typically shows a bat wing 4th ventricle and prominent thickened elongated superior cerebellar peduncles giving characteristic molar tooth sign1 like appearance.
In a minority of cases minor lateral ventriculomegaly (6 - 20% of cases), and corpus callosal dysgenesis (6 - 10% of cases) is also present 5.
Treatment and prognosis
Not an overwhelming amount of data is available on the long term outcome of children with Joubert syndrome. Persistent neuromotor developmental retardation is a feature of surviving individuals. Patients with associated retinal dysplasia appear to have a poorer prognosis 5.
Extreme care needs to be taken when administering any agent that causes respiratory depression, as individuals with Joubert syndrome are exquisitely sensitive to these effects 5.
Genetic counselling is required as the condition is autosomal recessive.
Etymology
It is named after the French neurologist : Marie Joubert who first described the condition in 1969
Differential diagnosis
- Dandy-Walker malformation :the Dandy-Walker continuum may also occur simultaneously with the Joubert anomaly in come cases
- rhombencephalosynapsis
- mega cisterna magna : no structural abnormality
-<p><strong>Joubert anomaly</strong> (also known as <strong>vermian aplasia </strong>or <strong>molar tooth midbrain-hindbrain malformation</strong>) is an autosomal recessive disorder where there is a variable degree of cerebellar vermal agenesis. </p><p>When associated with anomalies of the kidneys, liver and/or eyes then the term <a title="JSRD" href="/articles/joubert-syndrome-related-disorders-jsrd">Joubert syndrome and related disorders (JSRD)</a> is used. </p><h4>Epidemiology</h4><p>The prevalence of Joubert syndrome is approximately 1 in 100000. There are numerous associations which are variably present <sup>5</sup>:</p><ul>- +<p><strong>Joubert anomaly</strong> (also known as <strong>vermian aplasia </strong>or <strong>molar tooth midbrain-hindbrain malformation</strong>) is an autosomal recessive disorder where there is a variable degree of cerebellar vermal agenesis. </p><p>When associated with anomalies of the kidneys, liver and/or eyes then the term <a href="/articles/joubert-syndrome-related-disorders-jsrd">Joubert syndrome and related disorders (JSRD)</a> is used. </p><h4>Epidemiology</h4><p>The prevalence of Joubert syndrome is approximately 1 in 100000. There are numerous associations which are variably present <sup>5</sup>:</p><ul>
-</ul><p><strong style="font-size:1.5em; font-weight:bold; line-height:1em">Clinical presentation</strong></p><p>Affected individuals usually present with <a href="/articles/ataxia">ataxia</a> and have dysmorphic facies, global developmental delay, hypotonia, rapid breathing and <a href="/articles/oculomotor-apraxia">oculomotor apraxia</a>. There is significant range in the degree of cognitive impairment with IQ ranging form 30 to 80, although presence of speech and motor deficits makes assessment difficult <sup>7</sup>. </p><p>Typically, patients have nystagmus and inability of smooth pursuit of a moving object <sup>5</sup>.</p><h4>Pathology</h4><p>Joubert syndrome patients are a heterogeneous population in terms of genetics with some having a mutation of chromosome 9q34.3 - many do not <sup>4</sup>. At least 10 genes have been implicated, relating to subcellular organelle the primary cilium and basal body; as such JS is one of a number of related disorders known as <a href="/articles/missing">ciliopathies</a> <sup><font size="1">7,8</font></sup>. </p><p> </p><h4>Radiographic features</h4><p>Cross-sectional axial imaging demonstrates isolated abnormality of the <a href="/articles/cerebellum">cerebellum</a>, consisting of:</p><ul>- +</ul><h4>Clinical presentation</h4><p>Affected individuals usually present with <a href="/articles/ataxia">ataxia</a> and have dysmorphic facies, global developmental delay, hypotonia, rapid breathing and <a href="/articles/oculomotor-apraxia">oculomotor apraxia</a>. There is significant range in the degree of cognitive impairment with IQ ranging form 30 to 80, although presence of speech and motor deficits makes assessment difficult <sup>7</sup>. </p><p>Typically, patients have nystagmus and inability of smooth pursuit of a moving object <sup>5</sup>.</p><h4>Pathology</h4><p>Joubert syndrome patients are a heterogeneous population in terms of genetics with some having a mutation of chromosome 9q34.3 - many do not <sup>4</sup>. At least 10 genes have been implicated, relating to subcellular organelle the primary cilium and basal body; as such JS is one of a number of related disorders known as <a href="/articles/missing">ciliopathies</a> <sup>7,8</sup>. </p><p> </p><h4>Radiographic features</h4><p>Cross-sectional axial imaging demonstrates isolated abnormality of the <a href="/articles/cerebellum">cerebellum</a>, consisting of:</p><ul>
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