A First Case Report of Subependymoma in PTPN11 Mutation-Associated Noonan Syndrome

المؤلفون المشاركون

Boonyawat, Boonchai
Charoenpitakchai, Mongkon
Suwanpakdee, Piradee

المصدر

Case Reports in Neurological Medicine

العدد

المجلد 2019، العدد 2019 (31 ديسمبر/كانون الأول 2019)، ص ص. 1-3، 3ص.

الناشر

Hindawi Publishing Corporation

تاريخ النشر

2019-09-16

دولة النشر

مصر

عدد الصفحات

3

التخصصات الرئيسية

الطب البشري

الملخص EN

Noonan syndrome (NS) is an autosomal dominant disorder in some cases caused by PTPN11 mutations.

Since somatic mutations in PTPN11 are seen in several tumor types, NS which causes germline PTPN11 mutations are also increase the risk of hematologic malignancies and brain solid tumors.

However, the report of brain tumors in Noonan syndrome remains rather rare.

Here, we report the first case of an 11-year-old Thai boy with Noonan syndrome who presented with symptoms related to hydrocephalus secondary to subependymoma in the fourth ventricle, and PTPN11 mutation was identified in this patient.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Boonyawat, Boonchai& Charoenpitakchai, Mongkon& Suwanpakdee, Piradee. 2019. A First Case Report of Subependymoma in PTPN11 Mutation-Associated Noonan Syndrome. Case Reports in Neurological Medicine،Vol. 2019, no. 2019, pp.1-3.
https://search.emarefa.net/detail/BIM-1141344

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Boonyawat, Boonchai…[et al.]. A First Case Report of Subependymoma in PTPN11 Mutation-Associated Noonan Syndrome. Case Reports in Neurological Medicine No. 2019 (2019), pp.1-3.
https://search.emarefa.net/detail/BIM-1141344

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Boonyawat, Boonchai& Charoenpitakchai, Mongkon& Suwanpakdee, Piradee. A First Case Report of Subependymoma in PTPN11 Mutation-Associated Noonan Syndrome. Case Reports in Neurological Medicine. 2019. Vol. 2019, no. 2019, pp.1-3.
https://search.emarefa.net/detail/BIM-1141344

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references

رقم السجل

BIM-1141344