Shady Wafa

Khamis Mushait, Saudi Arabia

Last Updated: 09/26/2026

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Found 10 publications

Severe Pneumocystis jirovecii Pneumonia in an Apparently Immunocompetent Child Complicated by Acute Respiratory Distress Syndrome and Air Leak Syndrome: A Case Report and Literature Review.

Severe Pneumocystis jirovecii Pneumonia in an Apparently Immunocompetent Child Complicated by Acute Respiratory Distress Syndrome and Air Leak Syndrome: A Case Report and Literature Review.

Journal: Cureus
Published: April 03, 2026

Iron Deficiency Anemia Among Pediatric Celiac Disease Patients at the Armed Forces Hospital Southern Region: Prevalence, Predictors, and Outcomes.

Iron Deficiency Anemia Among Pediatric Celiac Disease Patients at the Armed Forces Hospital Southern Region: Prevalence, Predictors, and Outcomes.

Journal: Cureus
Published: February 12, 2026

A Novel Homozygous ITGA2B Variant Associated With Recurrent Epistaxis in a Four-Year-Old Girl: A Case Report.

A Novel Homozygous ITGA2B Variant Associated With Recurrent Epistaxis in a Four-Year-Old Girl: A Case Report.

Journal: Cureus
Published: February 03, 2026

A Male Child With Combined Glucose-6-Phosphate Dehydrogenase Deficiency and Hereditary Elliptocytosis: The First Case Reported From Saudi Arabia.

A Male Child With Combined Glucose-6-Phosphate Dehydrogenase Deficiency and Hereditary Elliptocytosis: The First Case Reported From Saudi Arabia.

Journal: Cureus
Published: November 25, 2025

First Reported Case of Glucose-6-Phosphate Isomerase Deficiency in a Saudi Child With Hemolytic Anemia.

First Reported Case of Glucose-6-Phosphate Isomerase Deficiency in a Saudi Child With Hemolytic Anemia.

Journal: Cureus
Published: October 17, 2025

Dehydrated Hereditary Stomatocytosis (DHS): A Rare Inherited Hemolytic Disorder With Unusual Hypochromic Microcytic Anemia.

Dehydrated Hereditary Stomatocytosis (DHS): A Rare Inherited Hemolytic Disorder With Unusual Hypochromic Microcytic Anemia.

Journal: Cureus
Published: March 27, 2025

Congenital Brucellosis: A Case Report and Literature Review.

Congenital Brucellosis: A Case Report and Literature Review.

Journal: Cureus
Published: February 25, 2025

Disseminated BCGitis with Interferon-Gamma Receptor Deficiency: An Example of an Extremely Rare Illness.

Disseminated BCGitis with Interferon-Gamma Receptor Deficiency: An Example of an Extremely Rare Illness.

Journal: Cureus
Published: February 06, 2025

Purine Nucleoside Phosphorylase Deficiency: A Case Report of an Extremely Rare Disorder.

Purine Nucleoside Phosphorylase Deficiency: A Case Report of an Extremely Rare Disorder.

Journal: Cureus
Published: December 22, 2024

Hermansky-Pudlak Syndrome Type 2: A Case Report on an Ultra-Rare Disorder.

Hermansky-Pudlak Syndrome Type 2: A Case Report on an Ultra-Rare Disorder.

Journal: Cureus
Published: July 22, 2024
Showing 1-10 of 10

Last Updated: 09/26/2026