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Neuromuscular disorder as initial manifestation of secondary hyperparathyroidism – a case report
Author(s) -
Karim Hajjar,
Tim Hagenacker
Publication year - 2017
Publication title -
european journal of translational myology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.271
H-Index - 6
eISSN - 2037-7460
pISSN - 2037-7452
DOI - 10.4081/ejtm.2017.6100
Subject(s) - medicine , weakness , parathyroid hormone , hyperparathyroidism , secondary hyperparathyroidism , muscle weakness , proximal muscle weakness , neurological examination , degeneration (medical) , pediatrics , endocrinology , surgery , pathology , biopsy , muscle biopsy , calcium
This case report describes a young woman who presented with slowly progressing weakness of the proximal limb muscles and slight decrease of muscle tone but otherwise unremarkable neurological history. Diagnostic workup revealed fatty degeneration of the girdle muscles and an excessive increase of the parathyroid hormone as a result of severe vitamin D deficiency. Secondary hyperparathyroidism was diagnosed, and neurological deficits resolved after treatment of the underlying endocrinopathy

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