Azzeddine Laaraje

Rabat, Morocco

Last Updated: 09/26/2026

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Found 13 publications

Deep Vein Thrombosis in an 11-Year-Old Child With Pulmonary Tuberculosis: A Case Report.

Deep Vein Thrombosis in an 11-Year-Old Child With Pulmonary Tuberculosis: A Case Report.

Journal: Cureus

Published: July 14, 2026

Diffuse Infantile Hepatic Hemangiomatosis: A Rare Cause of Consumptive Hypothyroidism.

Diffuse Infantile Hepatic Hemangiomatosis: A Rare Cause of Consumptive Hypothyroidism.

Journal: Cureus

Published: May 01, 2026

Griscelli Syndrome Type 2 Revealed by Macrophage Activation Syndrome: Two Cases From the Same Family.

Griscelli Syndrome Type 2 Revealed by Macrophage Activation Syndrome: Two Cases From the Same Family.

Journal: Cureus

Published: September 25, 2025

Novel ANKRD11 Mutation in KBG Syndrome: A diagnostic triad of hearing loss, radiological macrodontia and artificial intelligence-assisted facial phenotyping.

Novel ANKRD11 Mutation in KBG Syndrome: A diagnostic triad of hearing loss, radiological macrodontia and artificial intelligence-assisted facial phenotyping.

Journal: Sultan Qaboos University medical journal

Published: August 19, 2025

Novel MCT8 mutation: diagnostic value of T3/T4 ratio.

Novel MCT8 mutation: diagnostic value of T3/T4 ratio.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: August 09, 2025

Thymic Hyperplasia Mimicking Lymphoma in a Pediatric Patient: A Case Report.

Thymic Hyperplasia Mimicking Lymphoma in a Pediatric Patient: A Case Report.

Journal: Cureus

Published: July 21, 2025

Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay with Early-Onset Epilepsy and Novel Clinical Features: A rare entity from Morocco in the Middle East and North Africa region.

Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay with Early-Onset Epilepsy and Novel Clinical Features: A rare entity from Morocco in the Middle East and North Africa region.

Journal: Sultan Qaboos University medical journal

Published: February 11, 2025

Severe congenital hyperinsulinism with progressive neurological deterioration due to novel HADH-GHSR digenic mutations: the first case report.

Severe congenital hyperinsulinism with progressive neurological deterioration due to novel HADH-GHSR digenic mutations: the first case report.

Journal: Pediatric endocrinology, diabetes, and metabolism

Published: January 01, 2025

From growth hormone deficiency to Kleefstra-2 syndrome: diagnostic reassessment of treatment-refractory short stature.

From growth hormone deficiency to Kleefstra-2 syndrome: diagnostic reassessment of treatment-refractory short stature.

Journal: Pediatric endocrinology, diabetes, and metabolism

Published: January 01, 2025

Isolated leptomeningeal angiomatosis in Sturge-weber syndrome type III: A case report with distinctive neuroimaging features.

Isolated leptomeningeal angiomatosis in Sturge-weber syndrome type III: A case report with distinctive neuroimaging features.

Journal: Radiology case reports

Published: December 27, 2024

Epidemiology of Latent Tuberculosis in Moroccan Healthcare Workers: Prevalence Patterns and Predisposing Factors.

Epidemiology of Latent Tuberculosis in Moroccan Healthcare Workers: Prevalence Patterns and Predisposing Factors.

Journal: Cureus

Published: December 15, 2024

Familial multiple lipomatosis in a 13-year-old child.

Familial multiple lipomatosis in a 13-year-old child.

Journal: The Pan African medical journal

Published: October 03, 2017

Showing 1-12 of 13

Last Updated: 09/26/2026