Alakeel Abdullah
Dermatology, College of Medicine, King Saud University, Riyadh, SAU.
Cureus. 2020 May 16;12(5):e8159. doi: 10.7759/cureus.8159.
Hemimaxillary enlargement, asymmetry of the face, tooth abnormalities, and skin findings (HATS) syndrome, a rare developmental disorder, involves the first and second branchial arches and is characterized by hemimaxillary enlargement, abnormal appearance of skin and teeth, and facial asymmetry. It is generally detected at birth or during early childhood and is associated with unilateral abnormalities of the face, including the bones, teeth, gums, and skin. Becker nevus is the most common cutaneous manifestation of HATS syndrome. Although patients with HATS syndrome have been treated with various therapeutic regimens, no standard or definitive treatment regimen has been established. This study describes this rare condition in a 12-year-old girl.
半侧上颌骨增大、面部不对称、牙齿异常和皮肤表现(HATS)综合征是一种罕见的发育障碍,累及第一和第二鳃弓,其特征为半侧上颌骨增大、皮肤和牙齿外观异常以及面部不对称。它通常在出生时或幼儿期被发现,并与面部单侧异常有关,包括骨骼、牙齿、牙龈和皮肤。贝克尔痣是HATS综合征最常见的皮肤表现。尽管HATS综合征患者已接受了各种治疗方案,但尚未确立标准或明确的治疗方案。本研究描述了一名12岁女孩的这种罕见病症。