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Hypoparathyroidism and Fahr’s Syndrome: A Case Series
Fahr’s syndrome is defined by the presence of striato-pallido-dentate calcifications. It is a rare entity with clinical polymorphism, and it occurs in patients with dysparathyroidism, especially those with hypoparathyroidism. It must be distinguished from Fahr’s disease (FD), which is defined by the...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10350282/ https://www.ncbi.nlm.nih.gov/pubmed/37461775 http://dx.doi.org/10.7759/cureus.40502 |
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author | Berrabeh, Soumiya Messaoudi, Najoua Elmehraoui, Ouafae Assarrar, Imane Karabila, Ikram Jamal, Anouar Zeryouh, Nabila Rouf, Siham Latrech, Hanane |
author_facet | Berrabeh, Soumiya Messaoudi, Najoua Elmehraoui, Ouafae Assarrar, Imane Karabila, Ikram Jamal, Anouar Zeryouh, Nabila Rouf, Siham Latrech, Hanane |
author_sort | Berrabeh, Soumiya |
collection | PubMed |
description | Fahr’s syndrome is defined by the presence of striato-pallido-dentate calcifications. It is a rare entity with clinical polymorphism, and it occurs in patients with dysparathyroidism, especially those with hypoparathyroidism. It must be distinguished from Fahr’s disease (FD), which is defined by the presence of intracerebral calcifications without phosphocalcic metabolism abnormality. In this paper, we report the particulars of five patients diagnosed with Fahr’s syndrome revealed by neurological and cognitive disorders, seizures, and abnormal movements associated with tetany crisis. In all cases, brain imaging and biological examinations led to the diagnosis of Fahr’s syndrome related to hypoparathyroidism. The evolution was favorable after treatment. Fahr’s syndrome is a rare and serious condition for which treatment is simple and effective. Our observations shed light on the necessity of evaluating phosphocalcic metabolism and exploring cerebral calcifications in patients with neurological disorders. |
format | Online Article Text |
id | pubmed-10350282 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-103502822023-07-17 Hypoparathyroidism and Fahr’s Syndrome: A Case Series Berrabeh, Soumiya Messaoudi, Najoua Elmehraoui, Ouafae Assarrar, Imane Karabila, Ikram Jamal, Anouar Zeryouh, Nabila Rouf, Siham Latrech, Hanane Cureus Endocrinology/Diabetes/Metabolism Fahr’s syndrome is defined by the presence of striato-pallido-dentate calcifications. It is a rare entity with clinical polymorphism, and it occurs in patients with dysparathyroidism, especially those with hypoparathyroidism. It must be distinguished from Fahr’s disease (FD), which is defined by the presence of intracerebral calcifications without phosphocalcic metabolism abnormality. In this paper, we report the particulars of five patients diagnosed with Fahr’s syndrome revealed by neurological and cognitive disorders, seizures, and abnormal movements associated with tetany crisis. In all cases, brain imaging and biological examinations led to the diagnosis of Fahr’s syndrome related to hypoparathyroidism. The evolution was favorable after treatment. Fahr’s syndrome is a rare and serious condition for which treatment is simple and effective. Our observations shed light on the necessity of evaluating phosphocalcic metabolism and exploring cerebral calcifications in patients with neurological disorders. Cureus 2023-06-16 /pmc/articles/PMC10350282/ /pubmed/37461775 http://dx.doi.org/10.7759/cureus.40502 Text en Copyright © 2023, Berrabeh et al. https://creativecommons.org/licenses/by/3.0/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 author and source are credited. |
spellingShingle | Endocrinology/Diabetes/Metabolism Berrabeh, Soumiya Messaoudi, Najoua Elmehraoui, Ouafae Assarrar, Imane Karabila, Ikram Jamal, Anouar Zeryouh, Nabila Rouf, Siham Latrech, Hanane Hypoparathyroidism and Fahr’s Syndrome: A Case Series |
title | Hypoparathyroidism and Fahr’s Syndrome: A Case Series |
title_full | Hypoparathyroidism and Fahr’s Syndrome: A Case Series |
title_fullStr | Hypoparathyroidism and Fahr’s Syndrome: A Case Series |
title_full_unstemmed | Hypoparathyroidism and Fahr’s Syndrome: A Case Series |
title_short | Hypoparathyroidism and Fahr’s Syndrome: A Case Series |
title_sort | hypoparathyroidism and fahr’s syndrome: a case series |
topic | Endocrinology/Diabetes/Metabolism |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10350282/ https://www.ncbi.nlm.nih.gov/pubmed/37461775 http://dx.doi.org/10.7759/cureus.40502 |
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