Extrapontine Myelinolysis following Extreme Hypernatremia and Hyperosmolarity

المؤلفون المشاركون

Schwade, Jan-Niclas
Haftel, Lior
Rühe, Lars
Endmann, Matthias

المصدر

Case Reports in Pediatrics

العدد

المجلد 2019، العدد 2019 (31 ديسمبر/كانون الأول 2019)، ص ص. 1-5، 5ص.

الناشر

Hindawi Publishing Corporation

تاريخ النشر

2019-01-17

دولة النشر

مصر

عدد الصفحات

5

التخصصات الرئيسية

الطب البشري

الملخص EN

We present a case of a nearly 3-year-old girl who was admitted to hospital due to severe hypernatremia (196 mmol/l).

Her medical history included central hypothyreosis and growth hormone deficiency.

Rehydration and normalization of sodium was achieved according to guidelines.

On the fourth day of hospitalization, the patient developed tremor, ataxia, and rigor.

Cranial magnetic resonance imaging (cMRI) was performed and (mis)interpreted for meningoencephalitis, with corresponding diagnostic and therapeutic implications.

The patient had extrapontine myelinolysis.

The child recovered completely after hospitalization for nearly 2 weeks.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Schwade, Jan-Niclas& Haftel, Lior& Rühe, Lars& Endmann, Matthias. 2019. Extrapontine Myelinolysis following Extreme Hypernatremia and Hyperosmolarity. Case Reports in Pediatrics،Vol. 2019, no. 2019, pp.1-5.
https://search.emarefa.net/detail/BIM-1143755

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Schwade, Jan-Niclas…[et al.]. Extrapontine Myelinolysis following Extreme Hypernatremia and Hyperosmolarity. Case Reports in Pediatrics No. 2019 (2019), pp.1-5.
https://search.emarefa.net/detail/BIM-1143755

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Schwade, Jan-Niclas& Haftel, Lior& Rühe, Lars& Endmann, Matthias. Extrapontine Myelinolysis following Extreme Hypernatremia and Hyperosmolarity. Case Reports in Pediatrics. 2019. Vol. 2019, no. 2019, pp.1-5.
https://search.emarefa.net/detail/BIM-1143755

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references

رقم السجل

BIM-1143755