Fronto-nasal Encephalocele and Hypertelorism in a Newborn: Surgical Management and Case Report
Journal Title: Scholars Journal of Medical Case Reports - Year 2015, Vol 3, Issue 5
Abstract
Abstract: Encephalocele is described as a protrusion of cranial contents (meninges and brain tissue) through a congenital or acquired defect of the skull. Congenitalis is due to a multifactorial neural tube defect. In the prenatal period, the diagnosis is made by ultrasound and in the postnatal period by tomography and / or magnetic resonance imaging. The goal of surgical treatment is to reduce brain herniation and obtain a sealed closure of the dura and a proper coverage of the skin. In this paper we describe a case of fronto-nasal encephalocele and hypertelorism and surgical management. Keywords: Encephalocele, Neural tube defect, Hypertelorism, Surgical management.
Authors and Affiliations
Alejandro Rojas- Marroquín, Hugo Navarro Palencia, Javier Guzmán
MRI Evaluation of CVJ Anomalies: Report of 7 Cases
Occipitocervical junction is an important area of the spine. This paper reports 7 cases of Craniovertebral Junction (CVJ) anomalies. The prime objective of the study was to provide a vision to the importance of MR imagin...
Maple Syrup Urine Disease – A Rare Case Report
Maple syrup urine disease (MSUD) is an inborn error of metabolism. It is a rare autosomal recessive inheritance disorder.It occurs in 1 in180, 000 infants. It is due to the defect in the metabolism of branched chain amin...
An interesting case of a pyometra in a postmenopausal woman
Abstract: Menopause brings many changes in woman’s body. Due to loss of hormonal support she is susceptible for various infections. One of the dangerous infections amongst this is pyometra which is infection of uterus. A...
A rare case report:Kimura’s disease presenting as bilateral post auricular swellings in a young male.
Kimura disease (KD) is a chronic inflammatory disorder with angiolymphatic proliferation, usually affecting young men of Asian race but is rare in other races. The disease is characterized by a triad of painless subcutan...
Rathke's Cleft Cyst and Panhypopituitarism: Two Cases Report
Rathke's cleft cysts are benign, usually asymptomatic cystic epithelial congenital lesions. The symptomatic forms are exceptional with endocrine manifestations due to hypophyseal compression by the cyst. We present two c...