HIPOPARATIROIDISMO PEDIATRIA PDF

Primary hyperparathyroidism is an infrequent condition in infancy and is usually due to adenoma. It may be asymptomatic and is suspected when isolated hypercalcemia is detected in routine investigations. We describe the case of a year-old boy with hypercalcemia presenting as renal lithiasis. Gammagraphy with Cardiolite-Technetium 99 suggested an adenoma in the inferior right portion of the parathyroid.

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ABSTRACT - We report the case of a white male infant, 2 months-old, with tremor and hypertonia since 15 th day of life transferred to our service and diagnosed as seizures. At this time hypoparathyroidism was suspected and the additional investigation confirmed this suspect ion.

The neurologic examination revealed an irritable patient with marked extensor hypertonia and opisthotonos. The infant was given the oral calcium gluconate, magnesium chloride and colecalciferol daily to maintain a normal calcium concentration, but the control was very difficult.

The patient had an extend hospitalization of 6 months and death was due to repetitive infection. We discuss the clinical findings, imaging, EEG exam, differential diagnosis and treatment of this disorder. Volpe J. Neurology of newborn. Philadelphia: Saunders, Seth DP. Hypocalcemic seizures in neonates. Am J Emerg Med ; Endocrine disorders in current pediatric diagnosis and treatment.

Current pediatric diagnosis and treatment. Connecticut: Appleton Lange, Jones KL. Aicardi J, Arzimanoglou A. Treatment of the childhood epilepsy syndromes. The treatment of epilepsy. Oxford: Blackwell, Shewmon A. Dissociation between cortical discharges and ictal movements in neonatal seizures.

Ann Neurol ; A study of clinical pathological and eletroencephalografic features in full-term babies with a long-term follow-up. Pediatrics ; Aicardi J. Epilepsy in children, 2.

York:Raven Press, Alon U, Chan JC. Hypocalcemia from deficiency of and resistance to parathyroid hormone. Adv Pediatr ;; Aceito 1 Outubro Cristiane Rocha - R. Fax 11 - E-mail: cri. Services on Demand Journal.

Hypocalcemia and neonatal seizures: a rare case of congenital hypoparathyroidism ABSTRACT - We report the case of a white male infant, 2 months-old, with tremor and hypertonia since 15 th day of life transferred to our service and diagnosed as seizures. All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License.

Vergueiro, sl. How to cite this article.

ARONDA NYAKAIRIMA PDF

Pilares para el enfoque y tratamiento adecuado del paciente con hipoparatiroidismo

ABSTRACT - We report the case of a white male infant, 2 months-old, with tremor and hypertonia since 15 th day of life transferred to our service and diagnosed as seizures. At this time hypoparathyroidism was suspected and the additional investigation confirmed this suspect ion. The neurologic examination revealed an irritable patient with marked extensor hypertonia and opisthotonos. The infant was given the oral calcium gluconate, magnesium chloride and colecalciferol daily to maintain a normal calcium concentration, but the control was very difficult. The patient had an extend hospitalization of 6 months and death was due to repetitive infection. We discuss the clinical findings, imaging, EEG exam, differential diagnosis and treatment of this disorder.

ALCALOIDI DELLA VINCA PDF

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