Devi Basanti, Behera Binodini, Patro Sibasish, Pattnaik Subhransu S, Puhan Manas R
Department of Skin and VD, SCB Medical College, Cuttack, Odisha, India.
Indian J Dermatol. 2013 May;58(3):241. doi: 10.4103/0019-5154.110853.
Gorlin Syndrome, a rare genodermatosis, otherwise known as Nevoid basal cell carcinoma syndrome (NBCCS) is a multisystem disease affecting skin, nervous system, eyes, endocrine glands, and bones. It is characterized by multiple basal cell carcinomas, palmoplantar pits, jaw cysts, and bony deformities like kyphoscoliosis and frontal bossing. We would like to report a case of Gorlin syndrome with classical features, as this is a rare genodermatosis.
戈林综合征是一种罕见的遗传性皮肤病，又称痣样基底细胞癌综合征（NBCCS），是一种影响皮肤、神经系统、眼睛、内分泌腺和骨骼的多系统疾病。其特征为多发性基底细胞癌、掌跖凹、颌骨囊肿以及诸如脊柱后凸和额部隆突等骨骼畸形。我们想报告一例具有典型特征的戈林综合征病例，因为这是一种罕见的遗传性皮肤病。
