Extensive intracranial calcifications and focal epilepsy as the initial manifestation of pseudohypoparathyroidism in a child: a case report
This case represents an unusual presentation of pseudohypoparathyroidism in childhood, in which long-standing focal epilepsy and extensive intracranial calcifications constituted the predominant manifestations, in the absence of the classic phenotypic features of Albright hereditary osteodystrophy.