کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
8586257 1564689 2018 5 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Dentofacial characteristics in a child with Meier-Gorlin syndrome: A rare case report
ترجمه فارسی عنوان
مشخصات دندانی فاسیال در یک کودک مبتلا به سندرم مایر گورلین: گزارش یک مورد نادر است
کلمات کلیدی
موضوعات مرتبط
علوم پزشکی و سلامت پزشکی و دندانپزشکی بیهوشی و پزشکی درد
چکیده انگلیسی
Meier-Gorlin syndrome (MGS) is a rare autosomal recessive disorder characterized by the triad of microtia, absent or small patellae and short stature. The other associated clinical features may include developmental delay, congenital pulmonary emphysema, gastro-esophageal reflux, urogenital anomalies, such as cryptorchidism and feeding problems. The facial characteristics during childhood are typical, comprising of a small mouth with full lips and micrognathia/retrognathia. The condition is rare affecting about one to nine individuals per million. Mutation in the genes of pre-replication complex involved in DNA-replication is detected in the majority of patients. This impedes the cellular proliferation resulting in a reduction of total cell number and thereby retardation of overall growth. This case report describe the typical dentofacial characteristics in a 5 years old child affected with Meier-Gorlin syndrome along with other associated anomalies and a multidisciplinary approach for their management.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: The Saudi Dental Journal - Volume 30, Issue 3, July 2018, Pages 260-264
نویسندگان
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