Ullah Ghafoor, Shabbir Sidra, Marwat Hanniya, Faizullah Fahad, Qadir Maisan, Sardar Maryam
Department of Dermatology, Medical Teaching Institute, Hayatabad Medical Complex, Peshawar, Pakistan.
Department of Dermatology, Medical Teaching Institute, Khyber Teaching Hospital, Peshawar, Pakistan.
J Pak Med Assoc. 2025 Jun;75(6):970-973. doi: 10.47391/JPMA.20061.
Bardet-Biedl syndrome (BBS) is a disorder of primary ciliary dysfunction, having a wide range of systemic and dermatological manifestations. We report the case of a nine-year-old patient having multiple erythematous plaques over the dorsal surface of both feet, scalp seborrhoea,, keratosis pilaris, and polydactyly, associated with night blindness and central obesity. Initial workup correlated well with BBS reporting metabolic syndrome, retinal dystrophy, and gonadal dysfunction. Genetic testing for disease confirmation was not done due to the limited hospital resources. Multidisciplinary symptomatic management was carried out for the patient, along with counselling of the parents regarding possible complications of the disease. This case was reported at the Dermatology Department of Medical Teaching Institute-Hayatabad Medical Complex, Peshawar.
巴德-比德尔综合征(BBS)是一种原发性纤毛功能障碍性疾病,具有广泛的全身和皮肤表现。我们报告一例9岁患者,双足背有多个红斑性斑块、头皮脂溢性皮炎、毛发角化病和多指畸形,伴有夜盲症和中心性肥胖。初步检查结果与BBS相符,提示存在代谢综合征、视网膜营养不良和性腺功能障碍。由于医院资源有限,未进行疾病确诊的基因检测。对该患者进行了多学科对症治疗,并就该疾病可能的并发症对其父母进行了咨询。此病例在白沙瓦哈亚塔巴德医学中心医学教学研究所皮肤科报告。