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Biomedical subjects

R Mallet

Publications and source records attributed to R Mallet.

At least 19 recordsLinked to original sources

Grey matter correlates of minor physical anomalies in the AeSOP first-episode psychosis study.

BACKGROUND: Minor physical anomalies are more prevalent among people with psychosis. This supports a neurodevelopmental aetiology for psychotic disorders, since these anomalies and the brain are both ectodermally derived. However, little is understood about the brain regions implicated in this association. AIMS: To examine the relationship between minor physical anomalies and grey matter structure in a sample of patients with first-episode psychosis. METHOD: Sixty patients underwent assessment of minor physical anomalies with the Lane scale. High-resolution magnetic resonance images and voxel-based methods of image analysis were used to investigate brain structure in these patients. RESULTS: The total anomalies score was associated with a grey matter reduction in the prefrontal cortex and precuneus and with a grey matter excess in the basal ganglia, thalamus and lingual gyrus. CONCLUSIONS: Minor physical anomalies in a sample of patients with first-episode psychosis are associated with regional grey matter changes. These regional changes may be important in the pathogenesis of psychotic disorder.

Adolescent↗

[Acute epididymitis disclosing tertiary tuberculosis].

The authors report the case of a 50-year-old drinker and smoker presenting with isolated acute on chronic epididymitis, leading to the diagnosis of tertiary tuberculosis. This now exceptional case emphasizes the value of scrotal ultrasound and complementary investigations looking for other sites of tuberculosis.

Acute Disease↗

[Partial trisomy of chromosome 21 by maternal translocation t(15;21) (q26.2; q21)].

A balanced reciprocal translocation, t(15;21) (q262;q21) was observed in the mother and maternal grandfather of two patients. The propositus, who received the abnormal chromosome 15 from his mother, is trisomic for the distal part of chromosome 21, and his phenotype is that of classical trisomy 21. His sister, who is trisomic for the proximal part of 21q, is slightly retarded but developmentally normal otherwise.

Child, Preschool↗