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

Joint Authors

Boonyawat, Boonchai
Charoenpitakchai, Mongkon
Suwanpakdee, Piradee

Source

Case Reports in Neurological Medicine

Issue

Vol. 2019, Issue 2019 (31 Dec. 2019), pp.1-3, 3 p.

Publisher

Hindawi Publishing Corporation

Publication Date

2019-09-16

Country of Publication

Egypt

No. of Pages

3

Main Subjects

Medicine

Abstract 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.

American Psychological Association (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

Modern Language Association (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

American Medical Association (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

Data Type

Journal Articles

Language

English

Notes

Includes bibliographical references

Record ID

BIM-1141344