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Cytokine Storm Syndrome Responsive to IL-1 Inhibition in Trisomy 21

Case reports in pediatrics, 2024, Vol.2024, p.9946401

2024

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Beyond Infantile Hemangiomas: A Glimpse into Overlapping Rare Syndromes Emphasizing the Vigilant Screening for PHACE and LUMBAR Syndromes

Case reports in pediatrics, 2024, Vol.2024, p.7501793

2024

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Asymptomatic Esophageal Eosinophilia in an 11-Year-Old with Severe Persistent Asthma

Case reports in pediatrics, 2023-10, Vol.2023, p.1-3

2023

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Effect of Recombinant Human Growth Hormone Treatment in a Patient with Short Stature Associated with the Ring Chromosome 17 Syndrome

Case reports in pediatrics, 2023-09, Vol.2023, p.1-4

2023

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The Use of Amantadine in Treating Extrapyramidal Symptoms in Organophosphates Poisoning in a Child

Case reports in pediatrics, 2023-09, Vol.2023, p.1-3

2023

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Enzyme Replacement Therapy (ERT) on Heart Function Changes the Outcome in Patients with Infantile-Onset Pompe Disease: A Familial History

Case reports in pediatrics, 2023-02, Vol.2023, p.8470341-5

2023

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Congenital Tufting Enteropathy, a Rare Cause of Diarrhea and Malnourishment in Arab Child with Genetic and Histopathology Investigations

Case reports in pediatrics, 2023-01, Vol.2023, p.6301065-3

2023

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Ectopia Cordis as a Lethal Neonatal Condition: A Case Report from Bahrain and a Literature Review

Case reports in pediatrics, 2022-08, Vol.2022, p.1-5

2022

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Identification of a New Variant of the MBTPS1 Gene of the Kondo-Fu Type of Spondyloepiphyseal Dysplasia (SEDKF) in a Saudi Patient

Case reports in pediatrics, 2022-10, Vol.2022, p.1-5

2022

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Acute Rhabdomyolysis in a Child with Multiple Suspicious Gene Variants

Case reports in pediatrics, 2022-09, Vol.2022, p.1-5

2022

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A Case Report and Literature Review of Pseudo-TORCH Syndrome Type 2 (PTORCH2)

Case reports in pediatrics, 2022-10, Vol.2022, p.1-5

2022

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Intrauterine Limb Ischemia in Patient Heterozygous for the 677C>T) RS1801133 (Polymorphism of Methylenetetrahydrofolate Reductase MTHR Gene

Case reports in pediatrics, 2022-10, Vol.2022, p.1-6

2022

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Diplopia and Optic Disc Edema as the Ocular Manifestations of COVID-19 in a Seven-Year-Old Child

Case reports in pediatrics, 2022-06, Vol.2022, p.1-3

2022

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Concomitant MPZ and MFN2 Gene Variants and Charcot Marie Tooth Disease in a Boy: Clinical and Genetic Analysis—Literature Review

Case reports in pediatrics, 2022-04, Vol.2022, p.3793226-6

2022

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Juvenile Hemochromatosis due to a Homozygous Variant in the HJV Gene

Case reports in pediatrics, 2022-04, Vol.2022, p.7743748-4

2022

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Cardiac Calcified Amorphous Tumor in the Neonatal Period

Case reports in pediatrics, 2022-01, Vol.2022, p.9087597-3

2022

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Successful Treatment with Antibiotics Alone for Infant Rib Osteomyelitis

Case reports in pediatrics, 2022-01, Vol.2022, p.1-5

2022

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Obstructive Sleep Apnea with Paradoxical Vocal Cord Movement in Children during Sleep Endoscopy: Case Series

Case reports in pediatrics, 2020-07, Vol.2020, p.7380802-4

2020

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The Value of Imagistics in Early Diagnosis of Tuberous Sclerosis

Case reports in pediatrics, 2020-03, Vol.2020, p.1309184-4

2020

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Successful Liposteroid Therapy for a Recurrent Idiopathic Pulmonary Hemosiderosis with Down Syndrome

Case reports in pediatrics, 2020-04, Vol.2020, p.5292947-5

2020

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Congenital Cytomegalovirus Infection Presenting with Hyperbilirubinemia and Splenomegaly in a Term Infant with Trisomy 21

Case reports in pediatrics, 2020-02, Vol.2020, p.2534629-4

2020

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Extensive Epidermal Skin Loss Secondary to HSV Type One: Neonatal Management Challenges

Case reports in pediatrics, 2019-12, Vol.2019, p.2459219-5

2019

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Hemolytic Crisis following Naphthalene Mothball Ingestion in a 21-Month-Old Patient with Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency

Case reports in pediatrics, 2019-06, Vol.2019, p.1092575-3

2019

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Physiotherapy and Rehabilitation in a Child with Joubert Syndrome

Case reports in pediatrics, 2017-01, Vol.2017, p.8076494-7

2017

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Empedobacter brevis Meningitis in a Neonate: A Very Rare Case of Neonatal Meningitis and Literature Review

Case reports in pediatrics, 2016-01, Vol.2016, p.7609602-4

2016

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Cytokine Storm Syndrome Responsive to IL-1 Inhibition in Trisomy 21

Beyond Infantile Hemangiomas: A Glimpse into Overlapping Rare Syndromes Emphasizing the Vigilant Screening for PHACE and LUMBAR Syndromes

Asymptomatic Esophageal Eosinophilia in an 11-Year-Old with Severe Persistent Asthma

Effect of Recombinant Human Growth Hormone Treatment in a Patient with Short Stature Associated with the Ring Chromosome 17 Syndrome

The Use of Amantadine in Treating Extrapyramidal Symptoms in Organophosphates Poisoning in a Child

Enzyme Replacement Therapy (ERT) on Heart Function Changes the Outcome in Patients with Infantile-Onset Pompe Disease: A Familial History

Congenital Tufting Enteropathy, a Rare Cause of Diarrhea and Malnourishment in Arab Child with Genetic and Histopathology Investigations

Ectopia Cordis as a Lethal Neonatal Condition: A Case Report from Bahrain and a Literature Review

Identification of a New Variant of the MBTPS1 Gene of the Kondo-Fu Type of Spondyloepiphyseal Dysplasia (SEDKF) in a Saudi Patient

Acute Rhabdomyolysis in a Child with Multiple Suspicious Gene Variants

A Case Report and Literature Review of Pseudo-TORCH Syndrome Type 2 (PTORCH2)

Intrauterine Limb Ischemia in Patient Heterozygous for the 677C>T) RS1801133 (Polymorphism of Methylenetetrahydrofolate Reductase MTHR Gene

Diplopia and Optic Disc Edema as the Ocular Manifestations of COVID-19 in a Seven-Year-Old Child

Concomitant MPZ and MFN2 Gene Variants and Charcot Marie Tooth Disease in a Boy: Clinical and Genetic Analysis—Literature Review

Juvenile Hemochromatosis due to a Homozygous Variant in the HJV Gene

Cardiac Calcified Amorphous Tumor in the Neonatal Period

Successful Treatment with Antibiotics Alone for Infant Rib Osteomyelitis

Obstructive Sleep Apnea with Paradoxical Vocal Cord Movement in Children during Sleep Endoscopy: Case Series

The Value of Imagistics in Early Diagnosis of Tuberous Sclerosis

Successful Liposteroid Therapy for a Recurrent Idiopathic Pulmonary Hemosiderosis with Down Syndrome

Congenital Cytomegalovirus Infection Presenting with Hyperbilirubinemia and Splenomegaly in a Term Infant with Trisomy 21

Extensive Epidermal Skin Loss Secondary to HSV Type One: Neonatal Management Challenges

Hemolytic Crisis following Naphthalene Mothball Ingestion in a 21-Month-Old Patient with Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency

Physiotherapy and Rehabilitation in a Child with Joubert Syndrome

Empedobacter brevis Meningitis in a Neonate: A Very Rare Case of Neonatal Meningitis and Literature Review

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