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Seizures in an Arabian foal due to suspected prolonged transient neonatal hypoparathyroidism
Author(s) -
Schwarz B.,
van den Hoven R.
Publication year - 2012
Publication title -
equine veterinary education
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.304
H-Index - 31
eISSN - 2042-3292
pISSN - 0957-7734
DOI - 10.1111/j.2042-3292.2011.00268.x
Subject(s) - foal , hypocalcaemia , medicine , hypoparathyroidism , acetazolamide , calcium , epilepsy , calcium supplementation , anesthesia , surgery , pediatrics , archaeology , psychiatry , history
Summary This Case Report describes a 5‐week‐old male Arabian foal of Egyptian bloodline with generalised seizures due to hypocalcaemia. The laboratory changes in this foal were consistent with an abnormal regulation of calcium as occurs with hypoparathyroidism. Prolonged transient neonatal hypoparathyroidism as reported in man was suspected. The foal received oral calcium and vitamin D 3 supplementation combined with the calcium sparing diuretic carbonic anhydrase inhibitor acetazolamide. Calcium concentrations increased gradually over 6 months. In Arabian foals, especially those of Egyptian bloodline suffering suspected juvenile epilepsy, hypocalcaemia should be ruled out as a cause of seizures.