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Syndrome de Fahr secondaire à une hypoparathyroïdie primaire: à propos d’un cas
Fahr syndrome is a rare anatomo-clinic disease whose most common cause is primary or postoperative hypoparathyroidism. It is characterized by bilateral and symmetrical intracerebral calcifications located in the central gray nuclei, most often associated with phosphocalcium metabolism disorders. We...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The African Field Epidemiology Network
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5398258/ https://www.ncbi.nlm.nih.gov/pubmed/28450981 http://dx.doi.org/10.11604/pamj.2017.26.2.10689 |
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author | El Boukhrissi, Fatima Zoulati, Ghizlane En-nafaa, Issam Ouleghzal, Hassan Derrou, Sara Safi, Soumaya Bamou, Youssef Balouch, Lhoussine |
author_facet | El Boukhrissi, Fatima Zoulati, Ghizlane En-nafaa, Issam Ouleghzal, Hassan Derrou, Sara Safi, Soumaya Bamou, Youssef Balouch, Lhoussine |
author_sort | El Boukhrissi, Fatima |
collection | PubMed |
description | Fahr syndrome is a rare anatomo-clinic disease whose most common cause is primary or postoperative hypoparathyroidism. It is characterized by bilateral and symmetrical intracerebral calcifications located in the central gray nuclei, most often associated with phosphocalcium metabolism disorders. We here report the case of a 54-year old patient who had been treated for primary hypoparathyroidism for 20 years, presenting with amnesic disorders revealing Fahr syndrome secondary to hypoparathyroidism. |
format | Online Article Text |
id | pubmed-5398258 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The African Field Epidemiology Network |
record_format | MEDLINE/PubMed |
spelling | pubmed-53982582017-04-27 Syndrome de Fahr secondaire à une hypoparathyroïdie primaire: à propos d’un cas El Boukhrissi, Fatima Zoulati, Ghizlane En-nafaa, Issam Ouleghzal, Hassan Derrou, Sara Safi, Soumaya Bamou, Youssef Balouch, Lhoussine Pan Afr Med J Case Report Fahr syndrome is a rare anatomo-clinic disease whose most common cause is primary or postoperative hypoparathyroidism. It is characterized by bilateral and symmetrical intracerebral calcifications located in the central gray nuclei, most often associated with phosphocalcium metabolism disorders. We here report the case of a 54-year old patient who had been treated for primary hypoparathyroidism for 20 years, presenting with amnesic disorders revealing Fahr syndrome secondary to hypoparathyroidism. The African Field Epidemiology Network 2017-01-04 /pmc/articles/PMC5398258/ /pubmed/28450981 http://dx.doi.org/10.11604/pamj.2017.26.2.10689 Text en © Fatima El Boukhrissi et al. http://creativecommons.org/licenses/by/2.0/ The Pan African Medical Journal - ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report El Boukhrissi, Fatima Zoulati, Ghizlane En-nafaa, Issam Ouleghzal, Hassan Derrou, Sara Safi, Soumaya Bamou, Youssef Balouch, Lhoussine Syndrome de Fahr secondaire à une hypoparathyroïdie primaire: à propos d’un cas |
title | Syndrome de Fahr secondaire à une hypoparathyroïdie primaire: à propos d’un cas |
title_full | Syndrome de Fahr secondaire à une hypoparathyroïdie primaire: à propos d’un cas |
title_fullStr | Syndrome de Fahr secondaire à une hypoparathyroïdie primaire: à propos d’un cas |
title_full_unstemmed | Syndrome de Fahr secondaire à une hypoparathyroïdie primaire: à propos d’un cas |
title_short | Syndrome de Fahr secondaire à une hypoparathyroïdie primaire: à propos d’un cas |
title_sort | syndrome de fahr secondaire à une hypoparathyroïdie primaire: à propos d’un cas |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5398258/ https://www.ncbi.nlm.nih.gov/pubmed/28450981 http://dx.doi.org/10.11604/pamj.2017.26.2.10689 |
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