Pseudohypoparathyroidism Presenting with Ventricular Arrhythmia: A Case Report
Author(s) -
Sedat Işıkay,
İlyas Akdemir,
Kutluhan Yılmaz
Publication year - 2012
Publication title -
journal of clinical research in pediatric endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.566
H-Index - 35
eISSN - 1308-5735
pISSN - 1308-5727
DOI - 10.4274/jcrpe.476
Subject(s) - medicine , hypomagnesemia , pseudohypoparathyroidism , tetany , qt interval , brachydactyly , cardiac arrhythmia , cardiology , afterdepolarization , bigeminy , electrocardiography , creatine kinase , parathyroid hormone , endocrinology , calcium , atrial fibrillation , materials science , electrophysiology , repolarization , short stature , magnesium , metallurgy , ventricular tachycardia
Pseudohypoparathyroidism (PHP) is a rare disorder characterized by varying degrees of unresponsiveness to parathyroid hormone. Patients usually present with hypocalcemia-induced seizures or tetany, whereas no case of hypocalcemia-induced cardiac arrhythmia in PHP has been described to date. In this paper, we report the case of a male adolescent with PHP type 1a who presented with hypocalcemia-induced ventricular extrasystoles (bigeminy, trigeminy) and mild corrected QT interval prolongation. The patient had brachydactyly and his second fingers and toes were longer than the others, a finding consistent with PHP. Laboratory tests detected hypomagnesemia, as well as elevated levels of creatine kinase and lactate dehydrogenase. Ventricular arrhythmia and abnormal laboratory tests improved with calcium supplementation and vitamin D treatment. The findings in this patient suggest that hypomagnesemia may make patients with PHP more susceptible to hypocalcemia and may thus prompt a state of hypocalcemia-induced arrhythmia or other cardiac complications.
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