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1.
Indian Pediatr ; 2014 Mar; 51(3): 203-210
Article in English | IMSEAR | ID: sea-170543

ABSTRACT

Justification: Neonatal cholestasis is an important cause of chronic liver disease in young children. Late referral and lack of precise etiological diagnosis are reasons for poor outcome in substantial number of cases in India. There is a need to create better awareness among the pediatricians, obstetricians and primary care physicians on early recognition, prompt evaluation and referral to regional centers. Process: Eminent national faculty members were invited to participate in the process of forming a consensus statement. Selected members were requested to prepare guidelines on specific issues, which were reviewed by two other members. These guidelines were then incorporated into a draft statement, which was circulated to all members. A round table conference was organized; presentations, ensuing discussions, and opinions expressed by the participants were incorporated into the final draft. Objectives: To review available published data on the subject from India and the West, to discuss current diagnostic and management practices in major centers in India, and to identify various problems in effective diagnosis and ways to improve the overall outcome. Current problems faced in different areas were discussed and possible remedial measures were identified. The ultimate aim would be to achieve results comparable to the West. Recommendations: Early recognition, prompt evaluation and algorithm-based management will improve outcome in neonatal cholestasis. Inclusion of stool/urine color charts in well baby cards and sensitizing pediatricians about differentiating conjugated from the more common unconjugated hyperbilirubinemia are possible effective steps. Considering the need for specific expertise and the poor outcome in sub- optimally managed cases, referral to regional centers is warranted.

2.
Indian Pediatr ; 2008 Jun; 45(6): 507-9
Article in English | IMSEAR | ID: sea-11530

ABSTRACT

Leucocyte adhesion defect (LAD) is an inherited disorder of phagocytic function. It is characterized by inability of the leucocytes, in particular neutrophilis to migrate from the blood stream towards sites of inflammation. LAD -1 is characterized by the absence of b 2 integrins (CD 11 / CD18) on leucocytes. This disorder is characterized by delayed separation of the umbilical cord, recurrent severe infections, periodontitis, and delayed wound healing. We report an infant where the diagnosis was confirmed by flow cytometry.


Subject(s)
Humans , Infant , Leukocyte-Adhesion Deficiency Syndrome/diagnosis , Male
3.
Indian Pediatr ; 2006 Oct; 43(10): 908-10
Article in English | IMSEAR | ID: sea-12060

ABSTRACT

A case of hepatic hemangioendothelioma presenting as congestive cardiac failure in a neonate is reported. There was also evidence of platelet consumption. The case was managed successfully with oral prednisolone, resulting in improvement of symptoms and tumor regression over 3 months.


Subject(s)
Disease Progression , Female , Glucocorticoids/therapeutic use , Hemangioendothelioma/diagnosis , Humans , Infant, Newborn , Liver Neoplasms/diagnosis , Prednisolone/therapeutic use
4.
Indian Pediatr ; 2002 Nov; 39(11): 1058
Article in English | IMSEAR | ID: sea-7912
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