In Joubert syndrome, the "molar tooth" sign can be associated with several additional supra- and infratentorial malformations. Here we report on 3 subjects (2 siblings, 8-14 years of age) with Joubert syndrome, showing an abnormal thick bulging of the anterior profile of the mesencephalon causing a complete obliteration of the interpeduncular fossa. DTI revealed that the abnormal tissue consisted of an ectopic white matter tract with a laterolateral transverse orientation. Tractographic reconstructions support the hypothesis of impaired axonal guidance mechanisms responsible for the malformation. The 2 siblings were compound heterozygous for 2 missense variants in the TMEM67 gene, while no mutations in a panel of 120 ciliary genes were dete...
Joubert syndrome is an autosomal recessive condition characterized by hypotonia, ataxia, psychomotor...
Joubert syndrome is a rare neurological and developmental malfunction represented by decreased muscl...
In 1969, Joubert et al. studied a family where four of six children had a severe clinical condition ...
In Joubert syndrome, the "molar tooth" sign can be associated with several additional supra-And infr...
In Joubert syndrome, the "molar tooth" sign can be associated with several additional supra- and inf...
PURPOSE We performed a retrospective study in which we investigated malformations other than brainst...
The so-called molar tooth sign is the radiologic hallmark of JSRD. Joubert syndrome is a rare, most ...
Joubert syndrome is a disorder characterized by ataxia, developmental delay, oculomotor anomalies, a...
SUMMARY: The so-called molar tooth sign is the radiologic hallmark of JSRD. Joubert syndrome is a ra...
Joubert syndrome (JS) is a rare autosomal recessive central nervous system malformation characterize...
Joubert syndrome is a congenital cerebellar ataxia with autosomal recessive or X-linked inheritance,...
Joubert syndrome is a congenital cerebellar ataxia with autosomal recessive or X-linked inheritance,...
Abstract Joubert syndrome (JS) and related disorders (JSRD) are a group of developmental delay/multi...
Joubert syndrome (JS) is an inherited disorder characterized by transient episodic hyperpnea, ataxia...
Background: Joubert Syndrome (JS) is a rare autosomal recessive disorder characterised clinically by...
Joubert syndrome is an autosomal recessive condition characterized by hypotonia, ataxia, psychomotor...
Joubert syndrome is a rare neurological and developmental malfunction represented by decreased muscl...
In 1969, Joubert et al. studied a family where four of six children had a severe clinical condition ...
In Joubert syndrome, the "molar tooth" sign can be associated with several additional supra-And infr...
In Joubert syndrome, the "molar tooth" sign can be associated with several additional supra- and inf...
PURPOSE We performed a retrospective study in which we investigated malformations other than brainst...
The so-called molar tooth sign is the radiologic hallmark of JSRD. Joubert syndrome is a rare, most ...
Joubert syndrome is a disorder characterized by ataxia, developmental delay, oculomotor anomalies, a...
SUMMARY: The so-called molar tooth sign is the radiologic hallmark of JSRD. Joubert syndrome is a ra...
Joubert syndrome (JS) is a rare autosomal recessive central nervous system malformation characterize...
Joubert syndrome is a congenital cerebellar ataxia with autosomal recessive or X-linked inheritance,...
Joubert syndrome is a congenital cerebellar ataxia with autosomal recessive or X-linked inheritance,...
Abstract Joubert syndrome (JS) and related disorders (JSRD) are a group of developmental delay/multi...
Joubert syndrome (JS) is an inherited disorder characterized by transient episodic hyperpnea, ataxia...
Background: Joubert Syndrome (JS) is a rare autosomal recessive disorder characterised clinically by...
Joubert syndrome is an autosomal recessive condition characterized by hypotonia, ataxia, psychomotor...
Joubert syndrome is a rare neurological and developmental malfunction represented by decreased muscl...
In 1969, Joubert et al. studied a family where four of six children had a severe clinical condition ...