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DOI 10.1136/bcr-2014-208290

Медицинская библиотека · BMJ case reports · 2015

Vitamin D deficiency in a patient with HDR syndrome.

Kostoglou-Athanassiou Ifigenia, Stefanopoulos Dimitrios, Karfi Areti, Athanassiou Panagiotis

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Аннотация

The case of a patient with clinical symptoms, laboratory and imaging findings of hypoparathyroidism, sensorineural deafness, renal dysplasia HDR, or Barakat syndrome (hypoparathyroidism, deafness, renal dysplasia), and vitamin D deficiency, is presented. A Caucasian man aged 51 years with a history of chronic hypocalcaemia since childhood, was admitted with hypertonia of the body and extremities, and loss of consciousness. On admission, he was found to have severe hypocalcaemia, hyperphosphataemia, severe hypoparathyroidism, low serum magnesium and mild renal insufficiency. Calcium gluconate was administered intravenously supplemented with magnesium, and the patient recovered consciousness while clinical and laboratory findings improved. Evaluation revealed left renal aplasia and sensorineural deafness affecting both ears. Vitamin D deficiency was also present. He was given calcium and vitamin D supplements orally, and the hypocalcaemia was corrected. This case is described as it is an extremely rare case of HDR syndrome with concurrent vitamin D deficiency.

Для цитирования: Kostoglou-Athanassiou Ifigenia, Stefanopoulos Dimitrios, Karfi Areti, Athanassiou Panagiotis. Vitamin D deficiency in a patient with HDR syndrome.. BMJ case reports. 2015. DOI: 10.1136/bcr-2014-208290.

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