Increasing macrocephaly in a neonate
نویسندگان
چکیده
منابع مشابه
Increasing macrocephaly in a neonate.
Infantile macrocephaly has a myriad of causes including megalencephaly, intracranial mass, and CSF disturbance.1 An 8-week-old infant presented with increasing head circumference. Antenatal ultrasound was unremarkable, with biparietal diameter and head circumference on the 50th centile at 20 weeks’ gestation. At birth, head circumference was on the 90th centile; no other abnormalities were reco...
متن کاملMacrocephaly Syndromes
MACROCEPHALY SYNDROMES Charles A. Williams, MD INTRODUCTION Macrocephaly is defined as a head circumference which is greater than 2 standard deviations larger than the average for a given age and sex. It refers to an abnormally large head inclusive of the scalp, cranial bone and intracranial contents. Macrocephaly may be due to megalencephaly (true enlargement of the brain) or due to other cond...
متن کاملPulmonary hypertension and macrocephaly in a newborn.
Three weeks later, the boy was still tachypneic and needed supplemental oxygen and nasogastric tube feeding. Cardiac catheterization was performed and showed normal pulmonary arterial pressure but left ventricle dilatation and high-output (8.4 liters/min) cardiac failure. Distended veins coming from the brain were seen and subsequently magnetic resonance angiography of the neurocranium was perf...
متن کاملTesticular torsion in a neonate; a case report
The testicular torsion which is typically seen in prepuberty is very rare in the early neonatal period; prenatal diagnosis is difficult. Herein, we report a five day-old male neonate with swelling and erythema of the right scrotum. Following Doppler ultrasound suggestive of testicular torsion, surgical exploration was undertaken. There was gangrene of the right testis with discoloration and ne...
متن کاملFamilial Cleidocranial Dysplasia in a Neonate: A Case Report
Background: Cleidocranial dysplasia (CCD) is a rare inherited skeletal dysplasia, with an incidence of 1 case per 1000,000 individuals. It is a form of predominantly autosomal dominant inheritance and is associated with a mutation in runt related transcription factor-2 gene mapped on chromosome 6p21. This disease primarily affects the bones formed by intramembranous ossification and is characte...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Neurology
سال: 2003
ISSN: 0028-3878,1526-632X
DOI: 10.1212/01.wnl.0000085869.22589.a4