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Author: amit2k8pmch

Unlocking the Secrets of HARTNUP 2024
Posted in
  • METABOLIC DISORDER
  • Blog
  • GENETICS

Unlocking the Secrets of HARTNUP 2024

HARTNUP DISEASE OVERVIEW HARTNUP disease, a rare genetic disorder, has long puzzled medical experts with its … Unlocking the Secrets of HARTNUP 2024Read more

by amit2k8pmch•March 8, 2024May 23, 2024•0
Posted in
  • Blog
  • pediatrics immunology

Fanconi Anemia: best Mnemonics 2024

FANCONI ANEMIA OVERVIEW Fanconi Anemia (FA) is a rare genetic disorder characterized by bone marrow failure, … Fanconi Anemia: best Mnemonics 2024Read more

by amit2k8pmch•March 8, 2024July 2, 2024•0
Posted in
  • Blog

Hyper IgE Syndrome (job syndrome)- Unraveling the Mnemonic 2024

Hyper IgE Syndrome (job syndrome): quick overview Hyper IgE Syndrome, also known as Job Syndrome, is … Hyper IgE Syndrome (job syndrome)- Unraveling the Mnemonic 2024Read more

by amit2k8pmch•March 8, 2024May 23, 2024•0
Understanding Fragile X Syndrome: The FErTILe X Syndrome 2024
Posted in
  • pediatrics immunology

Understanding Fragile X Syndrome: The FErTILe X Syndrome 2024

Fragile X syndrome (FXS) Overview Fragile X syndrome (FXS) is a well-known genetic disorder characterized by … Understanding Fragile X Syndrome: The FErTILe X Syndrome 2024Read more

by amit2k8pmch•February 17, 2024May 24, 2024•1
Posted in
  • pediatrics immunology

LESCH-NYHAN DISEASE: MNEMONICS

Lesch-Nyhan Disease Lesch-Nyhan Disease, generally known as Lesch- Nyhan Syndrome or simply Lesch- Nyhan, is a … LESCH-NYHAN DISEASE: MNEMONICSRead more

by amit2k8pmch•February 8, 2024July 2, 2024•1
Understanding Bruton Agammaglobulinemia: Mnemonic BRETON and Management
Posted in
  • pediatrics immunology

Understanding Bruton Agammaglobulinemia: Mnemonic BRETON and Management

Bruton Agammaglobulinemia Bruton Agammaglobulinemia is a rare primary immunodeficiency disorder characterized by the absence or very … Understanding Bruton Agammaglobulinemia: Mnemonic BRETON and ManagementRead more

by amit2k8pmch•December 22, 2023June 22, 2024•3
Unraveling Common Variable Immunodeficiency (CVID): Pathophysiology and Clinical Manifestations
Posted in
  • pediatrics immunology

Unraveling Common Variable Immunodeficiency (CVID): Pathophysiology and Clinical Manifestations

Common Variable Immunodeficiency (CVID) Common Variable Immunodeficiency (CVID) is a primary immunodeficiency disorder characterized by impaired … Unraveling Common Variable Immunodeficiency (CVID): Pathophysiology and Clinical ManifestationsRead more

by amit2k8pmch•December 22, 2023June 22, 2024•2
Posted in
  • pediatrics immunology

Chediak-Higashi Syndrome (CHS):Unforgettable mnemonics 23

Chediak-Higashi Syndrome (CHS) Chediak-Higashi Syndrome (CHS) is a rare and complex autosomal recessive genetic disorder that … Chediak-Higashi Syndrome (CHS):Unforgettable mnemonics 23Read more

by amit2k8pmch•December 22, 2023May 23, 2024•0
Posted in
  • Blog
  • pediatrics immunology

Wiskott Aldrich Syndrome (WAS): Unforgettable Mnemonics 2023

Wiskott Aldrich Syndrome( WAS) Wiskott Aldrich Syndrome( WAS) is a rare X-linked primary immunodeficiency .WAS is … Wiskott Aldrich Syndrome (WAS): Unforgettable Mnemonics 2023Read more

by amit2k8pmch•December 21, 2023July 3, 2024•0
Posted in
  • Blog

METABOLIC DISORDERS MADE SIMPLE AND EASY 2023

DIFFERENT METABOLIC DISORDER WITH MNEMONICS Von-Gierke’s disease (type-1 glycogenosis characterized by recurrent hypoglycemia attacks with hepatomegaly, … METABOLIC DISORDERS MADE SIMPLE AND EASY 2023Read more

by amit2k8pmch•December 19, 2023March 8, 2024•0

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Recent Posts

  • Chronic Diarrhea in Children: Etiopathogenesis and Diagnostic Approach
  • Approach to Pyrexia of Unknown Origin (PUO) in Children: A Step-by-Step Clinical Guide
  • Precocious Puberty in Girls: Diagnostic Approach
  • 5 Key Insights: Diagnosing Congenital CMV in a Well-Appearing Infant with Petechiae and HSM
  • Malrotation of Gut in Neonates – A Pediatric Emergency You Must Not Miss

Recent Comments

  1. Chronic Diarrhea in Children: Etiopathogenesis and Diagnostic Approach - MASTERPEDIATRICS on Familial Anonychia: A Rare Case of Congenital Nail Dysplasia (congenital anonychia)in a Newborn with Paternal History
  2. Chronic Diarrhea in Children: Etiopathogenesis and Diagnostic Approach - MASTERPEDIATRICS on Diagnostic Algorithm for a Child with Failure to Thrive (FTT)
  3. Chronic Diarrhea in Children: Etiopathogenesis and Diagnostic Approach - MASTERPEDIATRICS on 10 Crucial Facts About Inflammatory Bowel Disease (IBD) in Children
  4. Severe Combined Immunodeficiency (SCID) Presenting as Persistent Fever with Persistent Leukocytosis and Lymphopenia in a 10-Month-Old Female: A Case Report - MASTERPEDIATRICS on Primary and secondary prevention of genetic disorders :Best article 2025
  5. Detailed Explanation of Iron Study Findings in Iron Deficiency Anemia (IDA) - MASTERPEDIATRICS on Effective Nocturnal Enuresis Treatments: From Motivational Therapy to Pharmacologic Interventions

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