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A Rare Observation of Brachymetacarpia and Brachymetatarsia in a Patient with Primary Idiopathic Hypoparathyroidism

Brachymetacarpia and brachymetatarsia are unique clinical entities associated with numerous rare conditions. Primary hypoparathyroidism is distinct from pseudohypoparathyroidism and pseudopseudohypoparathyroidism by lacking skeletal changes such as short metacarpals or metatarsals. Here, we present...

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Autores principales: Karunathilake, Parackrama, Rajaratnam, Arun, Kularatne, W. K. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9991468/
https://www.ncbi.nlm.nih.gov/pubmed/36895827
http://dx.doi.org/10.1155/2023/4149677
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author Karunathilake, Parackrama
Rajaratnam, Arun
Kularatne, W. K. S.
author_facet Karunathilake, Parackrama
Rajaratnam, Arun
Kularatne, W. K. S.
author_sort Karunathilake, Parackrama
collection PubMed
description Brachymetacarpia and brachymetatarsia are unique clinical entities associated with numerous rare conditions. Primary hypoparathyroidism is distinct from pseudohypoparathyroidism and pseudopseudohypoparathyroidism by lacking skeletal changes such as short metacarpals or metatarsals. Here, we present a case of a 64-year-old patient with brachymetacarpia and brachymetatarsia presented with hypocalcemic symptoms and signs, bilateral cataracts, and basal ganglia calcifications, subsequently diagnosed with idiopathic primary hypoparathyroidism. This is a rare case describing such an infrequent observation of brachymetacarpia and brachymetatarsia in primary idiopathic hypoparathyroidism.
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spelling pubmed-99914682023-03-08 A Rare Observation of Brachymetacarpia and Brachymetatarsia in a Patient with Primary Idiopathic Hypoparathyroidism Karunathilake, Parackrama Rajaratnam, Arun Kularatne, W. K. S. Case Rep Endocrinol Case Report Brachymetacarpia and brachymetatarsia are unique clinical entities associated with numerous rare conditions. Primary hypoparathyroidism is distinct from pseudohypoparathyroidism and pseudopseudohypoparathyroidism by lacking skeletal changes such as short metacarpals or metatarsals. Here, we present a case of a 64-year-old patient with brachymetacarpia and brachymetatarsia presented with hypocalcemic symptoms and signs, bilateral cataracts, and basal ganglia calcifications, subsequently diagnosed with idiopathic primary hypoparathyroidism. This is a rare case describing such an infrequent observation of brachymetacarpia and brachymetatarsia in primary idiopathic hypoparathyroidism. Hindawi 2023-02-28 /pmc/articles/PMC9991468/ /pubmed/36895827 http://dx.doi.org/10.1155/2023/4149677 Text en Copyright © 2023 Parackrama Karunathilake et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under 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
Karunathilake, Parackrama
Rajaratnam, Arun
Kularatne, W. K. S.
A Rare Observation of Brachymetacarpia and Brachymetatarsia in a Patient with Primary Idiopathic Hypoparathyroidism
title A Rare Observation of Brachymetacarpia and Brachymetatarsia in a Patient with Primary Idiopathic Hypoparathyroidism
title_full A Rare Observation of Brachymetacarpia and Brachymetatarsia in a Patient with Primary Idiopathic Hypoparathyroidism
title_fullStr A Rare Observation of Brachymetacarpia and Brachymetatarsia in a Patient with Primary Idiopathic Hypoparathyroidism
title_full_unstemmed A Rare Observation of Brachymetacarpia and Brachymetatarsia in a Patient with Primary Idiopathic Hypoparathyroidism
title_short A Rare Observation of Brachymetacarpia and Brachymetatarsia in a Patient with Primary Idiopathic Hypoparathyroidism
title_sort rare observation of brachymetacarpia and brachymetatarsia in a patient with primary idiopathic hypoparathyroidism
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9991468/
https://www.ncbi.nlm.nih.gov/pubmed/36895827
http://dx.doi.org/10.1155/2023/4149677
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