Posted in Research Article

Characteristics of Postpartum Japanese Mothers Who Were Nonrespondents to the Japan Environment and Children’s Study

Background: This study aimed to examine the factors behind survey non-response in mothers who had agreed to participate in a Japanese nationwide birth cohort study-…

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Posted in Mini Review

Breastfeeding vs. Infant Formula Feed: A Mini Review

Mothers’ milk provides best nutritional need for all infants. As a biologic fluid, it has kinds of benefits like, somatic growth, modulation of postnatal intestinal…

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Posted in Case Report

Hydroxychloroquine Does not Affect CTLA-4 Expression in LRBA Deficiency: Case Report from Siblings with LRBA Deficiency

Lipopolysaccharide-responsive and beige-like anchor protein (LRBA) deficiency is a rare autosomal recessive genetic disease that presents as a primary immunodeficiency and immune dysregulation caused by…

Continue Reading... Hydroxychloroquine Does not Affect CTLA-4 Expression in LRBA Deficiency: Case Report from Siblings with LRBA Deficiency
Posted in Research Article

Analysis of Follow-Up Results after Successful Conservative Treatment of Pediatric Appendiceal Abscess- A Single Institutional Retrospective Study

Purpose: The follow-up results of successful conservative treatment of appendiceal abscess in children were analyzed to further explore the value of interval appendectomy (IA).Method: Follow-up…

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Posted in Case Report

Hay Wells Syndrome: Report of an Extremely Rare Disorder

Hay-Wells syndrome also known as AEC syndrome (Ankyloblepharon-Ectodermal Dysplasia-clefting syndrome) is an uncommon form of ectodermal dysplasia initially described by Hay and Wells in 1976….

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Posted in Case Report

Novel Mutation in RAG2 Gene in a Patient with Severe Combined Immunodeficiency and BCG Infection: A Case Report

Severe Combined Immunodeficiency (SCID) represents a group of disorders characterised by impairment in both cellular and humoral immunity. SCID patients usually present severe and life-…

Continue Reading... Novel Mutation in RAG2 Gene in a Patient with Severe Combined Immunodeficiency and BCG Infection: A Case Report