Klippel-trenaunay and sturge-weber overlapping syndrome with craniofacial impairment: a case report

Klippel-Trenaunay syndrome (KTS) is characterized by a triad of port wine stains, venous malformations, and unilateral bone and/or tissue hypertrophy. Sturge-Weber syndrome (SWS) is a neurocutaneous syndrome of a classical triad of capillary malformations, ipsilateral leptomeningeal angiomatosis, and ocular involvement. The coexistence of KTS and SWS is rare, and only a few cases have been reported. Here, we describe a combination of KTS and SWS and report a case of a 27-year-old male patient, diagnosed with interictal dysphoric disorder, epilepsy, and mild intellectual disability.

Source: Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics - August 31, 2020 Category: ENT & OMF Authors: LETICIA RODRIGUES DE OLIVEIRA, GRAZIELA FIGUEREDO LIMA, RITA DE C ÁSSIA D´OTTAVIANO NÁPOLE, MARCELO IVANDER ANDRADE WANDERLEY, REYNALDO ANTEQUERA, BRUNA LUIZA ROIM VAROTTO Tags: 20190129 Source Type: research