aortic coarctation/seizures

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Cerebrovascular abnormalities in postoperative coarctation of aorta. Four cases demonstrating left subclavian steal on aortography.

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Identifikohuni Regjistrohu

Fifteen children, aged 0.3 to 10.5 years (mean 3.8 years) after repair of coarctation of the aorta, underwent cerebral arteriography as part of postoperative catheterization. Four manifested central nervous system symptoms postoperative catheterization. Four manifested central nervous system

Arch Augmentation via Median Sternotomy for Coarctation of Aorta With Proximal Arch Hypoplasia.

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Identifikohuni Regjistrohu

BACKGROUND Coarctation of the aorta can be associated with hypoplasia of the proximal transverse aortic arch. One approach to manage this condition is via left thoracotomy and extended end-to-end anastomosis with the expectation that the proximal arch will grow over time. Our preferred approach is

Contrast-induced seizures after cardiac catheterization in a 6-year-old child.

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Identifikohuni Regjistrohu

Neurologic complications of cardiac catheterization are usually embolic events resulting in stroke or seizures of vascular origin. Contrast-induced seizures have been rarely described in children. This report presents clinical, neuroimaging, and follow-up data of a 6-year-old female subjected to

Prenatal diagnosis of a fetus with congenital heart defect and ring chromosome 14.

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Identifikohuni Regjistrohu

Monosomy of chromosome 14 has been reported in only a few prenatal cases. Generally, this monosomy is associated with a mosaicism of ring chromosome 14. Ring chromosome 14 is a rare cytogenetic entity with clinical characteristics that include growth retardation, facial dysmorphia, hypotonia,

Characteristics and progression of hearing loss in children with turner's syndrome.

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Identifikohuni Regjistrohu

Evaluate patterns of hearing impairment in children with Turner's syndrome (TS) and determine factors influencing severity and progression.Retrospective database review.Demographic, audiological, and medical data for children

Schimmelpenning syndrome: an association with vascular anomalies.

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Identifikohuni Regjistrohu

OBJECTIVE Schimmelpenning syndrome is a rare neurocutaneous disorder characterized by craniofacial nevus sebaceus in association with seizures, developmental delay, and ocular or skeletal pathology. Vascular anomalies also have been described in this condition, and some authors have suggested that

18p deletion syndrome with a 45, XY, t (14; 18) (p11;q11.2), -18, karyotype.

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Identifikohuni Regjistrohu

A dysmorphic male child of 8 months age presented with microphthalmia, micrognathia, hypertelorism, wide anterior fontanelles, large forehead, short neck, prominent ears, macrotestis and delayed developmental milestones. The patient presented with generalised seizures hydrocephalaus and Coarctation

Elevated blood pressures in infants and children.

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Identifikohuni Regjistrohu

Blood pressure should be routinely measured in all infants and children. Measurements should be performed with an appropriate size cuff and observed pressures compared to normal values for age. Elevated blood pressure is seen in one to ten percent of children, depending on the age group surveyed and

Hypertension in the neonate.

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Identifikohuni Regjistrohu

Blood pressure (BP) is low at birth. It increases with age, by about 1 mm Hg per day within the period of 3 to 8 days. It rises by about 1 mm Hg per week between ages 5 to 6 weeks. At a latter age, systolic BP is close to 95 +/- 10 mm Hg. Hypertension is a rare condition in the neonate, where it

Hypertension secondary to renal hypoplasia presenting as acute heart failure in a newborn.

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Identifikohuni Regjistrohu

Neonatal hypertension is defined as persistent systolic and/or diastolic blood pressures above the 95th percentile compared to other infants of similar gestational age and size. Neonatal hypertension is a rare condition, occurring in only 0.2-3.0% of neonates. The most common etiology

Arterial hypertension in the newborn infant.

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Identifikohuni Regjistrohu

Blood pressure is low at birth. It increases with age by about 1 mm Hg per day within the period of 3-8 days. It rises by about 1 mm Hg per week between 5 and 6 weeks of age. Neonatal hypertension carries a risk of cardiorespiratory failure and cerebral distress. Causes of neonatal hypertension are

Moyamoya syndrome associated with congenital heart disease.

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Identifikohuni Regjistrohu

OBJECTIVE To describe the association between moyamoya syndrome and congenital heart disease and to discuss its clinical implications. Study Design. Retrospective analysis of a case series from two institutions. RESULTS Five patients with moyamoya syndrome and structural congenital heart disease

[Renovascular hypertension in childhood].

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Identifikohuni Regjistrohu

One to two per cent of children and up to 11% of adolescent have arterial hypertension. In most cases children and adolescent are not recognized to be hypertensive because physicians do not routinely measure blood pressure. Often the diagnosis is recognized only when the pediatric patients develop a

Neonatal neoplasms.

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Identifikohuni Regjistrohu

OBJECTIVE To describe neoplasms diagnosed in children

[Pulmonary vein stenosis. Report of 2 cases and review of the literature].

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Identifikohuni Regjistrohu

Topical congenital pulmonary vein stenosis is a uncommon defect, both isolated or associated to other cardiac abnormalities. Only the localization of the lesions seems to affect the survival, because 60% of survival cases has unilateral stenosis; the severity of associated cardiac lesions become the

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