Intraperitoneal metoclopramide causing a movement disorder
نویسندگان
چکیده
منابع مشابه
Clinical Course of Six Children With GNAO1 Mutations Causing a Severe and Distinctive Movement Disorder.
OBJECTIVES Mutations in GNAO1 have been described in 11 patients to date. Although most of these individuals had epileptic encephalopathy, four patients had a severe movement disorder as the prominent feature. We describe the largest series of patients with de novoGNAO1 mutations who have severe chorea, developmental delay, and hypotonia in the absence of epilepsy. METHODS Six patients with r...
متن کاملTraumatic Injury Causing Intraperitoneal Hemorrhage of an Occult Pheochromocytoma
Pheochromocytoma is a rare catecholamine-secreting tumor derived from chromaffin cells. The diagnosis is usually suggested by classic history in a symptomatic patient, presence of a strong family history in a patient, or discovery of an incidental mass on imaging in an asymptomatic patient. Traumatic hemorrhage into an occult pheochromocytoma presenting as hypovolemic shock is a rare presentati...
متن کاملMovement disorder emergencies.
Movement disorders may present acutely, and failure to recognize and exclude important differential diagnoses can result in significant morbidity or mortality. Unfortunately, much of the literature pertaining to this topic is scattered and not easily accessible. This review aims to address this deficit. Movement disorder emergencies are discussed according to their most likely mode of presentat...
متن کاملMovement Disorder Emergencies
Movement disorders are neurologic disorders characterized by inadequate voluntary movements (hypokinetic) or presence of abnormal involuntary movements (hyperkinetic). Management of either type of movement disorders is mainly outpatient-based . Movement disorder emergencies are conditions evolving over hours to days , in which failure to diagnose and manage promptly can result in significant mo...
متن کاملAn Interesting Case of a Movement Disorder.
Neuroacanthocytosis is a genetic neurodegenerative disorder with syndromes of variable inheritance. These hyperkinetic movement disorders are reported to be very rare. It is associated with choreiform movements, orofacial and lingual dyskinesias and acanthocytes on peripheral smear and normolipoproteinemia. Here we present a similar case.
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Nephrology Dialysis Transplantation
سال: 2002
ISSN: 1460-2385
DOI: 10.1093/ndt/17.5.945