Spectrum of clinical manifestations in Turkish patients with Williams-Beuren Syndrome: A monocentric studySemra Gürsoy1, Filiz Hazan2, Cüneyt Zihni3, Sezer Acar4, Murat Muhtar Yılmazer3, Timur Meşe3, Behzat Özkan41Department of Pediatric Genetics, Dr.Behcet Uz Child Disease and Pediatric Surgery Training and Research Hospital, Izmir, Turkey 2Department of Medical Genetics, Dr.Behcet Uz Child Disease and Pediatric Surgery Training and Research Hospital, Izmir, Turkey 3Department of Pediatric Cardiology, Dr.Behcet Uz Child Disease and Pediatric Surgery Training and Research Hospital, Izmir, Turkey 4Department of Pediatric Endocrinology, Dr.Behcet Uz Child Disease and Pediatric Surgery Training and Research Hospital, Izmir, Turkey
INTRODUCTION: Williams–Beuren syndrome, which is characterized by dysmorphic facial features, cardiovascular findings, intellectual disability, endocrine abnormalities and a typical cognitive profile, is caused by a microdeletion in the 7q11.23 region. In this study, we aimed to evaluate the dysmorphic and clinical manifestations of patients with Williams-Beuren syndrome. METHODS: We, retrospectively, collected data from 27 Turkish patients who had clinically and genetically confirmed Williams-Beuren syndrome. The multisystemic manifestations, demographic data and dysmorphic facial features were recorded. RESULTS: All patients had the characteristic facial phenotype. The most frequent dysmorphic facial features were periorbital fullness, short nose, broad nasal tip and wide mouth. Aortic stenosis (59.2%) and pulmonary stenosis (37%) were the most common cardiac findings. Short stature (25.9%), idiopathic central precocious puberty (7.4%), hypothyroidism (congenital, non-congenital or subclinical) (40.7%) and hypercalcaemia (3.7%) were the major endocrine manifestations in the patients. Genitourinary abnormalities were detected in 6 patients. All patients had some degree of intellectual disability; most of the patients (62.9%) had mild intellectual disability. Besides, behavioral problems were frequently detected and the most common abnormality was overfriendliness (77.7%). Renal abnormalities (double collecting system, bladder diverticulae and renal calculi) were also detected. DISCUSSION AND CONCLUSION: Dysmorphic facial features, which have a crucial role in the diagnosis of Williams-Beuren syndrome, should be assessed in suspected patients with supravalvular aortic stenosis and concomitant intellectual disability, to make an early diagnosis. It should be kept in mind that endocrine abnormalities, musculoskeletal, neurologic and psychiatric manifestations are also common in patients with Williams-Beuren syndrome, necessitating multidisciplinary approach.
Keywords: Williams-Beuren syndrome, 7q11.23 deletion, supravalvular aortic stenosis, pulmonary stenosis, intellectual disability
Semra Gürsoy, Filiz Hazan, Cüneyt Zihni, Sezer Acar, Murat Muhtar Yılmazer, Timur Meşe, Behzat Özkan. Spectrum of clinical manifestations in Turkish patients with Williams-Beuren Syndrome: A monocentric study. . 2021; 8(3): 0-0
Corresponding Author: Semra Gürsoy, Türkiye |
|