Javascript must be enabled to continue!
Acute Necrotizing Encephalopathy in 3 Brothers
View through CrossRef
Acute necrotizing encephalopathy (ANE) is a devastating and rapidly progressive neurologic disorder that occurs in healthy children after common viral infections. Typically, ANE is sporadic and does not recur. However, familial (ANE1) and recurrent cases have been reported and were recently linked to mutations in RANBP2 (RAN-binding protein 2). We report here a multiply affected kindred with recurrent familial ANE. These affected male siblings (a set of twins and their older brother) all presented with prodromal fever and upper respiratory tract infection that progressed within 72 hours to seizures, coma, and ultimately death, a course that is typical of ANE. It should be noted that 1 brother was treated with early aggressive management, including corticosteroids, and he survived for an additional 5 years. This represents the second reported case of familial ANE in the United States and the only case of male siblings with consanguineous parents. We hope that early recognition and growing awareness can lead to more effective treatment and better outcomes in the future.
American Academy of Pediatrics (AAP)
Title: Acute Necrotizing Encephalopathy in 3 Brothers
Description:
Acute necrotizing encephalopathy (ANE) is a devastating and rapidly progressive neurologic disorder that occurs in healthy children after common viral infections.
Typically, ANE is sporadic and does not recur.
However, familial (ANE1) and recurrent cases have been reported and were recently linked to mutations in RANBP2 (RAN-binding protein 2).
We report here a multiply affected kindred with recurrent familial ANE.
These affected male siblings (a set of twins and their older brother) all presented with prodromal fever and upper respiratory tract infection that progressed within 72 hours to seizures, coma, and ultimately death, a course that is typical of ANE.
It should be noted that 1 brother was treated with early aggressive management, including corticosteroids, and he survived for an additional 5 years.
This represents the second reported case of familial ANE in the United States and the only case of male siblings with consanguineous parents.
We hope that early recognition and growing awareness can lead to more effective treatment and better outcomes in the future.
Related Results
Oral Manifestation of Sexual Transmitted Diseases
Oral Manifestation of Sexual Transmitted Diseases
Abstract: Sexually transmitted diseases (STDs) are transmitted through sexual contact, and can manifest in the oral cavity. This study aimed to determine the oral manifestations of...
Encefalopati uremikum pada pasien gagal ginjal: Laporan kasus
Encefalopati uremikum pada pasien gagal ginjal: Laporan kasus
Background: Patients with kidney failure often experience clinical symptoms related to fluid and electrolyte imbalance, anemia, malnutrition, and gastrointestinal disorders. One of...
Slaveri hos Tuaregerne i Sahara
Slaveri hos Tuaregerne i Sahara
Slavery among the Tuareg in the SaharaA preliminary analysis of its structure.Slavery is an institution of very considerable age. In Europe and the Orient it has been common for as...
Reduced Serum Cholinesterase Activity Distinguishes Hepatic Encephalopathy From 48 Types of Human Diseases
Reduced Serum Cholinesterase Activity Distinguishes Hepatic Encephalopathy From 48 Types of Human Diseases
Abstract
Background: Hepatic encephalopathy is a complication of central nervous systems due to liver failure-related brain inflammation. Less than half of patients sufferi...
Assessment of Serum Biochemical Changes in Hepatic Encephalopathy
Assessment of Serum Biochemical Changes in Hepatic Encephalopathy
Objective: To analyze the association of various biochemical changes with different grades of hepatic encephalopathy among patients of hepatitis C-related decompensated liver disea...
Frequency of Recurrence of Hepatic Encephalopathy in Patients of Chronic Liver Disease Treated With Rifaximin
Frequency of Recurrence of Hepatic Encephalopathy in Patients of Chronic Liver Disease Treated With Rifaximin
Aim: To determine the frequency of recurrence of hepatic encephalopathy in patients treated with Rifaximin. Study design: Observational cross-sectional study. Setting & duratio...
Minimal Hepatic Encephalopathy is an under Recognized Entity in Clinical Practice of Bangladeshi Physician
Minimal Hepatic Encephalopathy is an under Recognized Entity in Clinical Practice of Bangladeshi Physician
Background: Minimal Hepatic Encephalopathy, the mildest from of Hepatic Encephalopathy is characterized by subtle motor and cognitive deficits and impairs health related quality of...
Frequency of Left Plueral Effusion in Acute Necrotizing Pancreatitis
Frequency of Left Plueral Effusion in Acute Necrotizing Pancreatitis
Objective: The aim of this study is to calculate the prevalence of left plueral effusion in acute necrotizing pancreatitis. Study Design: Observational/ case series Place and Dura...

