دورية أكاديمية

TP63 mutation mapping information in TP63 mutation-associated syndromes

التفاصيل البيبلوغرافية
العنوان: TP63 mutation mapping information in TP63 mutation-associated syndromes
المؤلفون: Yosuke Harazono, Kei-ichi Morita, Erina Tonouchi, Eri Anzai, Namiaki Takahara, Tomohiro Kohmoto, Issei Imoto, Tetsuya Yoda
المصدر: Advances in Oral and Maxillofacial Surgery, Vol 5, Iss , Pp 100253- (2022)
بيانات النشر: Elsevier, 2022.
سنة النشر: 2022
المجموعة: LCC:Internal medicine
LCC:Surgery
مصطلحات موضوعية: TP63, TP63 mutation-associated syndromes, Rapp-Hodgkin syndrome, EEC syndrome, Genotype-phenotype discrepancy, Internal medicine, RC31-1245, Surgery, RD1-811
الوصف: The transcription factor tumour protein 63, encoded by the TP63 gene, is a regulator of epidermal development. Heterozygous mutations in TP63 cause a variety of human ectodermal dysplasia disorders, including ankyloblepharon-ectodermal defects-cleft lip/palate syndrome, ectrodactyly, ectodermal dysplasia, cleft lip/palate syndrome, split hand/foot malformation 4, Rapp-Hodgkin syndrome, limb mammary syndrome, and acro-dermato-ungual-lacrimal-tooth syndrome. There are genotype-phenotype correlations in some of these syndromes, and the number of cases with overlapping symptoms has been increasing. The phenotypic spectrum and expressivity of TP63 mutation-associated syndromes complicate its clinical diagnosis and classification. Here, we present an updated review of TP63 mutation mapping information, together with a comprehensive overview of TP63 mutation-associated syndromes. We show that several cases with the same mutation have been previously diagnosed with different syndromes. This study will be useful for the diagnosis and classification of TP63 mutation-associated syndromes.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2667-1476
العلاقة: http://www.sciencedirect.com/science/article/pii/S2667147622000036Test; https://doaj.org/toc/2667-1476Test
DOI: 10.1016/j.adoms.2022.100253
الوصول الحر: https://doaj.org/article/202363e211234e5797f81ff133603ee7Test
رقم الانضمام: edsdoj.202363e211234e5797f81ff133603ee7
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:26671476
DOI:10.1016/j.adoms.2022.100253