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Manifestations parkinsoniennes révélant un syndrome de Fahr : à propos d'un cas.

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Introduction : Le syndrome de Fahr est une entité anatomoclinique rare, associant une calcification des noyaux gris centraux de manière symétrique à un tableau neuropsychiatrique très varié. Il est le plus souvent diagnostiqué à un âge jeune. L'objectif de cette étude était de rapporter un cas de syndrome de Fahr révélé par des manifestations parkinsoniennes.Observation : Nous rapportons le cas d'une patiente âgée de 73 ans reçue en consultation pour suspicion d'une maladie de Parkinson. Le scanner cérébral montrait des calcifications bilatérales et symétriques des noyaux gris centraux. Le bilan biologique mettait en évidence une dysparathyroïdie. Le diagnostic de syndrome de Fahr secondaire à une hypovitaminose D a été retenu. L'évolution clinique était favorable sous supplémentation vitamino-calcique.Conclusion : Le syndrome de Fahr est une pathologie rare. Il doit être évoqué devant des calcifications symétriques des noyaux gris à la tomodensitométrie associées à une perturbation du phosphocalcique. AbstractIntroduction: Fahr's syndrome is a rare anatomoclinical entity, associating a dysparathyroidism, calcification of the basal ganglia symmetrically with a very varied neuropsychiatric intracerebral picture. It is most often diagnosed at a young age. The objective of this study was to calcifications, report a case of Fahr syndrome revealed by parkinsonian manifestations. parkinsonism Observation: We report the case of a 73-year-old patient received for consultation on suspicion of Parkinson's disease. The brain scan showed bilateral and symmetrical calcifications of the basal ganglia. The biological assessment revealed dysparathyroidism. The diagnosis of Fahr syndrome secondary to hypovitaminosis D was retained. The clinical course was favorable with vitamin-calcium supplementation. Conclusion: Fahr syndrome is a rare pathology. It should be considered in front of symmetrical calcifications of the gray nuclei on the tomodensitometry associated with disturbance of the phosphocalcic.
Title: Manifestations parkinsoniennes révélant un syndrome de Fahr : à propos d'un cas.
Description:
Introduction : Le syndrome de Fahr est une entité anatomoclinique rare, associant une calcification des noyaux gris centraux de manière symétrique à un tableau neuropsychiatrique très varié.
Il est le plus souvent diagnostiqué à un âge jeune.
L'objectif de cette étude était de rapporter un cas de syndrome de Fahr révélé par des manifestations parkinsoniennes.
Observation : Nous rapportons le cas d'une patiente âgée de 73 ans reçue en consultation pour suspicion d'une maladie de Parkinson.
Le scanner cérébral montrait des calcifications bilatérales et symétriques des noyaux gris centraux.
Le bilan biologique mettait en évidence une dysparathyroïdie.
Le diagnostic de syndrome de Fahr secondaire à une hypovitaminose D a été retenu.
L'évolution clinique était favorable sous supplémentation vitamino-calcique.
Conclusion : Le syndrome de Fahr est une pathologie rare.
Il doit être évoqué devant des calcifications symétriques des noyaux gris à la tomodensitométrie associées à une perturbation du phosphocalcique.
 AbstractIntroduction: Fahr's syndrome is a rare anatomoclinical entity, associating a dysparathyroidism, calcification of the basal ganglia symmetrically with a very varied neuropsychiatric intracerebral picture.
It is most often diagnosed at a young age.
The objective of this study was to calcifications, report a case of Fahr syndrome revealed by parkinsonian manifestations.
parkinsonism Observation: We report the case of a 73-year-old patient received for consultation on suspicion of Parkinson's disease.
The brain scan showed bilateral and symmetrical calcifications of the basal ganglia.
The biological assessment revealed dysparathyroidism.
The diagnosis of Fahr syndrome secondary to hypovitaminosis D was retained.
The clinical course was favorable with vitamin-calcium supplementation.
Conclusion: Fahr syndrome is a rare pathology.
It should be considered in front of symmetrical calcifications of the gray nuclei on the tomodensitometry associated with disturbance of the phosphocalcic.

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