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http://www.ncbi.nlm.nih.gov/pubmed/25825851

Van Biervliet S, Küry S, De Bruyne R, Vanakker OM, Schmitt S, VandeVelde S,Blouin E, Bézieau S. Clinical zinc deficiency as early presentation of Wilsondisease. J PediatrGastroenterolNutr. 2015;60(4):457-9.

Abstract
Wilson disease is a rare autosomal recessive disorder of the copper metabolism caused by homozygous or compound heterozygous mutations in the ATP-aseCu(2+) transporting polypeptide (ATP7B) gene. The copper accumulation in different organs leads to the suspicion of Wilson disease. We describe a child with clinical zinc deficiency as presenting symptom of Wilson disease, which was confirmed by 2 mutations within the ATP7B gene and an increased copper excretion.

Published on: 
Apr-2015

http://www.ncbi.nlm.nih.gov/pubmed/25631669

Angeli P, Gines P, Wong F, Bernardi M, Boyer TD, Gerbes A, Moreau R, Jalan R, Sarin SK, Piano S, Moore K, Lee SS, Durand F, Salerno F, Caraceni P, Kim WR, Arroyo V, Garcia-Tsao G. Diagnosis and management of acute kidney injury in patients with cirrhosis: revised consensus recommendations of the International Club of Ascites. Gut. 2015; 64(4):531-7.

Published on: 
Apr-2015

 

What is Hepatoblastoma?

Hepatoblastoma is a rare tumor of liver. It is however the most common cancerous liver tumor in early childhood. Usually affects children younger than 3 years more so younger than 18 months. The frequency is more in low birth weight babies.

http://www.ncbi.nlm.nih.gov/pubmed/25557690

Sanyal AJ, Friedman SL, McCullough AJ, Dimick-Santos L. Challenges andopportunities in drug and biomarker development for nonalcoholic steatohepatitis: Findings and recommendations from an American Association for the Study of Liver Diseases-U.S. Food and Drug Administration Joint Workshop. Hepatology. 2015; 61(4):1392-405.

Abstract

Published on: 
Apr-2015

http://www.ncbi.nlm.nih.gov/pubmed/24944144

Mekala S, Jagadisan B, Parija SC, Lakshminarayanan S. Surveillance for infectious complications in pediatric acute liver failure - a prospective study. Indian J Pediatr. 2015 Mar; 82(3):260-6.

Abstract
OBJECTIVE:
To prospectively evaluate infectious complications (IC) in pediatric acute liver failure (PALF) by employing surveillance cultures.

METHODS:
From 2011 to 2013, children with PALF in a tertiary care centre received a standard protocolised management. Prophylactic parenteral antibiotics were used without antifungals. Surveillance cultures of blood, urine, ascites and tracheal aspirates were sent. Biochemical and clinical parameters and outcomes were compared between children with and without IC.

RESULTS:

Published on: 
Mar-2015

http://www.ncbi.nlm.nih.gov/pubmed/24928107

Sabat J, Dwibedi B, Dash L, Kar SK. Occult HBV infection in multi transfused thalassemia patients. Indian J Pediatr. 2015 Mar; 82(3):240-4.

Abstract

OBJECTIVE:
To determine the prevalence of Hepatitis B virus (HBV) and Hepatitis C virus (HCV) infection in multitransfused thalassemic patients, with an aim to further highlight the need for donor screening strategy with supplementary molecular diagnostic tools for high risk population.

METHODS:
The study was conducted in 174 thalassemic subjects from Thalassemia unit of Central Red Cross Blood Bank, Cuttack, Odisha, India. Sero molecular diagnosis was followed to detect antigen, antibody and DNA in the study subjects.

RESULTS:

Published on: 
Mar-2015

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