El-Moataz Bellah Ahmed Nermeen, Mostafa Mostafa I, Abdel-Hamid Mohamed S, Mehrez Mennat
Oro-dental Genetics Department, Egypt.
Medical Molecular Genetics Department, Egypt.
Saudi Dent J. 2024 Sep;36(9):1209-1214. doi: 10.1016/j.sdentj.2024.07.001. Epub 2024 Jul 2.
GAPO syndrome is usually diagnosed clinically owing to its characteristic features of growth retardation, alopecia, pseudoanodontia, and ophthalmic anomalies. Pseudoanodontia describes the failure of eruption of the two sets of teeth in these patients. Thus, the abnormal dental phenotype is the emergence of a set or part of a set of dentitions.
This study reports the physical, oro-dental, and molecular findings of two new sibs with GAPO syndrome and provides a description of the dental phenotype of one of the patients reported before.
MATERIALS & METHODS: The patients were subjected to full medical history taking and three generations-pedigree construction. They were phenotyped according to the elements of morphology: Standard terminology series. After parental consents were acquired, molecular analysis was carried out for the two sibs (Patient 1 & 2).
These included a new gene variant associated with erupted teeth in GAPO syndrome and new clinical features. A new classification for the terminologies of eruption disturbances was suggested.
The study asserts the importance of oro-dental examination and follow-ups as dental updates may occur in these cases.
GAPO综合征通常因其生长发育迟缓、脱发、假性无牙症和眼部异常等特征而通过临床诊断。假性无牙症指的是这些患者两组牙齿萌出失败。因此,异常的牙齿表型是一组或部分牙列的出现。
本研究报告了两名患有GAPO综合征的新同胞的身体、口腔牙齿和分子学检查结果,并对之前报道的一名患者的牙齿表型进行了描述。
对患者进行了全面的病史采集和三代系谱构建。根据形态学要素对他们进行表型分析:标准术语系列。在获得家长同意后,对两名同胞(患者1和患者2)进行了分子分析。
这些结果包括与GAPO综合征中萌出牙齿相关的一个新基因变异和新的临床特征。提出了一种关于萌出障碍术语的新分类。
该研究强调了口腔牙齿检查和随访的重要性,因为在这些病例中可能会出现牙齿方面的新情况。