Chiari type I malformation of infants and toddlers

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چکیده

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Chiari I malformation and neurofibromatosis type 1.

Single case reports exist in the medical literature of patients with tonsillar ectopia, i.e., the Chiari I malformation and neurofibromatosis type 1. However, large series of patients with either of these entities have not been examined for the presence of both defects. We have retrospectively examined two large groups of pediatric patients: Group I, with the primary diagnosis of Chiari I malfo...

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Orthostatic intolerance and syncope associated with Chiari type I malformation.

The Chiari type I malformation (CM1) is characterized by herniation of cerebellar tonsils to at least 3-5 mm below the plane of foramen magnum and can present with a wide variety of clinical symptoms, frequently including occipital headaches, secondary to bulbar and/or medullary distress. Rarely, syncopal episodes have also been described and attributed to either compression of the midbrain asc...

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Osteopetrosis and Chiari type I malformation: a rare association

Osteopetrosis (OP) is hereditary X-linked, autosomal recessive (ARO), or autosomal dominant (ADO) skeletal disease. ARO has two subtypes, which are infantile malignant and intermediate type. ARO and X-linked OP have poor clinical outcome. ADO is called adult benign type because of the normal life expectancy, which has type I and type II. Here, the authors present an ADO patient with Chiari type...

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Delirium, headache, and the type I Arnold-Chiari malformation.

Acute delirium can occur in a variety of states including migraine, l head trauma,2 nonconvulsive status epilepticus,3 and cerebral infarction.4 Acute delirium accompanied by migrainous headache is much more common in children than adults and is termed acute confusional migraine.s In 1883 John Cleland, a British poet and anatomist, first described the abnormality of the brainstem and cerebellum...

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ژورنال

عنوان ژورنال: Child's Nervous System

سال: 2018

ISSN: 0256-7040,1433-0350

DOI: 10.1007/s00381-017-3712-7