A DEAF CHILD WITH HYPOPARATHYROIDISM: A CASE REPORT

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FALAH RAZIEH; SHAJARI A.

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Journal: QOM UNIVERSITY OF MEDICAL SCIENCES JOURNAL Year:2010 | Volume:4 | Issue:1 Page(s): 48-53

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Title

A DEAF CHILD WITH HYPOPARATHYROIDISM: A CASE REPORT

Author(s)

FALAH RAZIEH | SHAJARI A. | Issue Writer Certificate

Keywords

SEIZURESQ2

HYPOCALCEMIAQ3

HYPOPARATHYROIDISMQ3

DEAFNESSQ3

Abstract

Background and Objectives: HDR (hypoparathyroidism DEAFNESS and renal dysplasia) is an autosomal dominant syndrome due to mutation in the glutamyl aminotransferase. We report a deaf child with HYPOPARATHYROIDISM. Case Report: The patient was a 6.5 year-old boy whose hearing impairment had been detected in infancy and cochlear implant had been done at 3.5 years of age. He had no problem until one week before admission when he faced carpopedal spasm and eyes-staring and he was then admitted to the hospital due to his status of epilepticus. Brain CT scan showed calcifications in frontal lobe and basal ganglia. HYPOCALCEMIA hyperphosphatemia and low parathyroid hormone level were detected in laboratory data. Kidney sonography was normal. Concerning negative family history and normal kidneys autosomal recessive form of disease without renal involvement or new mutation might be suggested in this patient; therefore in deaf patients HYPOPARATHYROIDISM would be taken into account.

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APA: Copy

FALAH, RAZIEH, & SHAJARI, A.. (2010). A DEAF CHILD WITH HYPOPARATHYROIDISM: A CASE REPORT. QOM UNIVERSITY OF MEDICAL SCIENCES JOURNAL, 4(1), 48-53. SID. https://sid.ir/paper/132458/en

Vancouver: Copy

FALAH RAZIEH, SHAJARI A.. A DEAF CHILD WITH HYPOPARATHYROIDISM: A CASE REPORT. QOM UNIVERSITY OF MEDICAL SCIENCES JOURNAL[Internet]. 2010;4(1):48-53. Available from: https://sid.ir/paper/132458/en

IEEE: Copy

RAZIEH FALAH, and A. SHAJARI, “A DEAF CHILD WITH HYPOPARATHYROIDISM: A CASE REPORT,” QOM UNIVERSITY OF MEDICAL SCIENCES JOURNAL, vol. 4, no. 1, pp. 48–53, 2010, [Online]. Available: https://sid.ir/paper/132458/en

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