Chiari I Malformation Causing Developmental Regression in a 4 Month Old

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Chiari I Malformation Causing Developmental Regression in a 4 Month Old

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Chiari I malformation and delivery

The following recommendations have been adopted and field tested on the patients of our centers for more than 10 years. They reflect the feedback from experts in the field of Obstetrics and Anesthesia, as well as the evolution of our understanding of CMI and syringomyelia. • A trial of natural childbirth is not contraindicated in patients with CMI (untreated, or after surgical decompression) • ...

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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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Chiari Malformation Type I: A Case-Control Association Study of 58 Developmental Genes

Chiari malformation type I (CMI) is a disorder characterized by hindbrain overcrowding into an underdeveloped posterior cranial fossa (PCF), often causing progressive neurological symptoms. The etiology of CMI remains unclear and is most likely multifactorial. A putative genetic contribution to CMI is suggested by familial aggregation and twin studies. Experimental models and human morphometric...

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Apnoeic episodes in a patient with Chiari type I malformation.

There can be a wide variety of symptoms in these patients, including headache, weakness, numbness of the limbs, unsteadiness and loss of balance.2 A variety of respiratory disorders have been described including acute respiratory failure,2 respiratory arrest I and sleep apnoea.' It is extremely unusual for a patient with the condition to have no abnormal neurological signs on presentation, ifap...

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ژورنال

عنوان ژورنال: Global Pediatric Health

سال: 2014

ISSN: 2333-794X,2333-794X

DOI: 10.1177/2333794x14560819