Macrodactyly in the context of tuberous sclerosis complex (TSC) is a known but rare
manifestation. We report the case of a boy diagnosed with TSC at 2 years and 4 months of …

3. METHODS When we saw his face, we realized that mask ventilation might be difficult
because his upper lip was markedly swollen and protruded due to angiomas. Therefore, we …

Wiedemann‐Steiner syndrome (WDSTS) is an exceptionally rare autosomal dominant
syndrome with considerable phenotypical variation. Clinical features include dysmorphic …

Sturge-Weber syndrome (SWS) is a neurocutaneous syndrome with vascular lesions of the
cerebral meninges, port wine spots on the face, and glaucoma of the eyes; it is a congenital …

Ossifying fibroma is a nonneoplastic developmental disease of osseous tissue seen rarely in
association with Sturge–Weber syndrome. It is a lesion of unknown aetiology, uncertain …

Résumé Le but était d'étudier l'apport du scanner dans la prise en charge des angiomatoses
lepto-méningées à propos de deux cas et de rapporter les difficultés rencontrées par nos …

Background: Hemihypertrophy is a condition in which one side or part of the body is larger
than the other. The asymmetry can range from mild to severe. It is important to establish a …

Vascular anomalies are a heterogeneous group of congenital blood vessel disorders more
typically referred to as “birthmarks.” They are further categorized into vascular tumors and …

Introdução: A síndrome de Sturge-Weber, também chamada de Angiomatose
Encefalotrigeminal, é uma doença congénita rara (1 em 20 000-50 000 nados-vivos) que …

Objective: The aim of this study was to report two cases of female patients diagnosed with
Sturge-Weber syndrome (SWS), its main oral and maxillofacial clinicals manifestations and …