DOI: 10.36347/sjmcr.2024.v12i06.021

Pages: 1053-1055

Gorlin-Goltz syndrome, also known as basal cell nevus syndrome. This condition is characterized by various clinical manifestations, including multiple cutaneous lesions and other systemic abnormalities. We present the case of a 32-year-old man with no significant medical history who was referred to our institution for evaluation of multiple budding lesions. Clinical examination revealed three lesions in the upper right nasolabial fold, one in the lower right cheek, one in the left nasolabial fold, and additional suspect lesions on the chin, right temple, and right cheek. This case underscores the importance of recognizing the diverse manifestations of Gorlin-Goltz syndrome, which can aid in early diagnosis and management of this inherited disorder. Further investigation and long-term follow-up are essential for understanding the progression and management of this condition.