Masamitsu Hyodo, Takahiko Yamagata, Kazumi Motoyoshi and Aki Taguchi Recurrent laryngeal nerve paralysis in children is a relatively rare disease. Its clinical features in children are considered dissimilar to those in adults. Here we present 11 cases of children with recurrent laryngeal nerve paralysis and discuss the manner of treatment for this disease. Clinical features compared and found t...

Congenital tracheal stenosis (CTS) is a serious and rare condition. In most cases, stenotic lesions are composed of complete tracheal rings of cartilage.The severity of symptoms correlates with the length of affected trachea, the presence of concomitant respiratory conditions, degree of luminal narrowing,and any bronchial involvement. Critically, CTS is a disorder that can lead to life-threaten...

INTRODUCTION Pompe disorder is a rare glycogen storage disorder that is due to a deficiency of the lysosomal alpha glycosidase enzyme. The heart, skeletal muscle, liver and nervous system can be affected from the lysosomal glycogen accumulation. Symptoms such as muscle weakness, hypotony, myopathy and respiratory failure develop. The onset may be at the infantile, adolescent or adult period dep...

Sleep-related respiratory disorders are highly prevalent, and represent a growing subspecialty of respiratory medicine. Sleep apnoea is nearly as prevalent in the general population as chronic obstructive pulmonary disease [1, 2], and the comprehensive management of the disorder requires special knowledge and expertise. Since sleep apnoea also represents the most common organic cause of excessi...

Introduction: As a standard measure in some chronic liver disorder, liver transplantation (LT) has performed for about 3 decades in pediatric populations. Post operatively some patients suffering from infectious complications by viral, bacterial and fungal etiologies. Here in we presented 10 children diagnosed as bacterial sinusitis presenting with prolonged fever and upper respiratory tract sy...

Pompe disease, also termed glycogen storage disease type II or acid maltase deficiency, caused by deficient activity of acid alpha-glucosidase (GAA), the glycogen degrading lysosomal enzyme. As a result, massive lysosomal glycogen deposits in the numerous organs including the muscles. In Pompe disease weakness of truncal muscles is a prominent presentation which results in respiratory failure a...

Computed Tomography (CT) is a non-invasive method to give CT images of every part the human body without superimposition end-to-end structures. Some issues in measurements with are limiting too few parameters like quantum noise, beam hardening, X-ray scattering by patient, and nonlinear partial volume effects. Image processing Adobe Photoshop, ImageJ, Origin software have been used achieve good...

OBJECTIVE The authors present a profile of panic disorder based on and generalized from the effects of acute and chronic hyperventilation that are characteristic of the respiratory panic disorder subtype. The review presented attempts to integrate three premises: hyperventilation is a physiological response to hypercapnia; hyperventilation can induce panic attacks; chronic hyperventilation is a...

The quantification of adenosine deaminase (ADA) in porcine saliva samples has been analyzed for its use as a marker of disease. First, an analytical validation of the enzymatic assay used for ADA measurements was performed. Afterwards, saliva samples were collected from 50 healthy animals and 64 animals with different symptoms of disease, which were divided into local inflammation, gastrointest...

BACKGROUND There has recently been increased interest in the relationship between physical illness, mental illness, and suicide. The present study utilizes a large community-based sample to investigate the association between certain physical conditions and suicidal behavior, among those with a history of a mood disorder. METHODS Data came from the nationally representative German Health Surv...