Javascript must be enabled to continue!
Essential palatal myoclonus with spontaneous resolution: a rare case report
View through CrossRef
Introduction and Importance:
Palatal myoclonus is a rare movement disorder characterized by involuntary, jerky movements of the soft palate and palatal musculature. It can be broadly divided into two types: essential palatal myoclonus (EPM) and symptomatic palatal myoclonus (SPM). In this case report we report a rare case of essential palatal myoclonus in pediatric patient which resolved on its own during follow-up.
Case Presentation:
A 8-year-old male presented with upper respiratory symptoms, with further examinations and investigations led to the diagnosis of essential palatal myoclonus. The patient had no accompanying neurological symptoms and brain imaging revealed no distinct lesions. The presentation was incidental and was resolved spontaneously within one year.
Clinical Discussion:
This case reports a rare occurrence of essential palatal myoclonus in pediatric patient. Careful clinical assessment is required to differentiate with symptomatic palatal myoclonus and brain imaging also helps to rule out any brain pathologies leading to palatal myoclonus.
Conclusion:
This case report contributes to scant pediatric literature on EPM and emphasize the need of clinicians to understand the benign nature in order to prevent unnecessary investigations and treatment.
Ovid Technologies (Wolters Kluwer Health)
Title: Essential palatal myoclonus with spontaneous resolution: a rare case report
Description:
Introduction and Importance:
Palatal myoclonus is a rare movement disorder characterized by involuntary, jerky movements of the soft palate and palatal musculature.
It can be broadly divided into two types: essential palatal myoclonus (EPM) and symptomatic palatal myoclonus (SPM).
In this case report we report a rare case of essential palatal myoclonus in pediatric patient which resolved on its own during follow-up.
Case Presentation:
A 8-year-old male presented with upper respiratory symptoms, with further examinations and investigations led to the diagnosis of essential palatal myoclonus.
The patient had no accompanying neurological symptoms and brain imaging revealed no distinct lesions.
The presentation was incidental and was resolved spontaneously within one year.
Clinical Discussion:
This case reports a rare occurrence of essential palatal myoclonus in pediatric patient.
Careful clinical assessment is required to differentiate with symptomatic palatal myoclonus and brain imaging also helps to rule out any brain pathologies leading to palatal myoclonus.
Conclusion:
This case report contributes to scant pediatric literature on EPM and emphasize the need of clinicians to understand the benign nature in order to prevent unnecessary investigations and treatment.
Related Results
Hydatid Disease of The Brain Parenchyma: A Systematic Review
Hydatid Disease of The Brain Parenchyma: A Systematic Review
Abstarct
Introduction
Isolated brain hydatid disease (BHD) is an extremely rare form of echinococcosis. A prompt and timely diagnosis is a crucial step in disease management. This ...
Breast Carcinoma within Fibroadenoma: A Systematic Review
Breast Carcinoma within Fibroadenoma: A Systematic Review
Abstract
Introduction
Fibroadenoma is the most common benign breast lesion; however, it carries a potential risk of malignant transformation. This systematic review provides an ove...
Chest Wall Hydatid Cysts: A Systematic Review
Chest Wall Hydatid Cysts: A Systematic Review
Abstract
Introduction
Given the rarity of chest wall hydatid disease, information on this condition is primarily drawn from case reports. Hence, this study systematically reviews t...
Hydatid Cyst of The Orbit: A Systematic Review with Meta-Data
Hydatid Cyst of The Orbit: A Systematic Review with Meta-Data
Abstarct
Introduction
Orbital hydatid cysts (HCs) constitute less than 1% of all cases of hydatidosis, yet their occurrence is often linked to severe visual complications. This stu...
SGCE Myoclonus Dystonia: A Case Report
SGCE Myoclonus Dystonia: A Case Report
BACKGROUND: SGCE myoclonus dystonia is a rare genetic movement disorder caused by mutations in the SGCE gene. It typically presents in childhood and is characterized by myoclonus a...


