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Introduction and aims: Submucous cleft palate (SMCP) is a congenital craniofacial malformation. While TBX22 is a known pathogenic gene, the potential role of TBX15 in SMCP remains unclear. This study aimed to investigate...

Speech quality is an essential output in assessing the success of a palatoplasty. The goal of a palatoplasty is not merely to create a simple anatomical closure of the palate, but also to create an adequate velopharyngea...

ABSTRACT Congenital cleft palate is the most described malformation in dogs, especially in purebred puppies. It is characterized by abnormal communication between the oral and nasal cavities through an opening in the pal...

Background/Aim: Congenital defects such as cleft palate and lips require a long-lasting and multidisciplinary approach. In cases when surgical and orthodontic treatment is not feasible, prosthodontic management of these ...

Cleft is a congenital abnormal space or gap in the upper lip, alveolus, or palate. This congenital abnormality occurs between the 5th and 10th weeks of pregnancy. Clefts are divided into cleft lip, cleft palate, as well ...

Cleft lip and palate are the most common craniofacial anomalies in Indonesia. Recent publications report that there was delayed skeletal and dental age in cleft lip and palate patients. Panoramic and lateral cephalometri...

Cleft lip and palate is one of the most common congenital anomalies. Cleft lip and palate patients encounter growth problems in lip and palate area, although their overall growth and development remains unknown. Cervical...

Abstract Little is known about the regulation and function of phase separation in craniofacial developmental disorders. MSX1 mutations are associated with human cleft palate, the most common craniofacial birth defect. He...

Latar Belakang: pada penderita palato schisis (celah langit-langit)yang disebkan hereditary atau bawaan lahir terlihat defect yang menyebabkan gangguan bicara (sengau), penelanan, pengunyahan, estetik, dan psikologis. Un...

IntroductionOromandibular limb hypogenesis syndrome (OLHS) Type IIIA is an exceptionally rare congenital anomaly, with only a few cases documented in the literature. It is characterized by developmental hypoplasia of the...

Abstract Background Congenital malformations in domestic cats are traditionally considered uncommon; however, recent evidence suggests they may represent an underrecognized cause of neonatal mortality. Most reported anom...

Kasus bibir dan lelangit sumbing merupakan salah satu kelainan deformitas yang sering terjadi. Keadaan klinis bervariasi mulai dari kasus sumbing tidak komplit sampai dengan komplit. Keadaan klinis dengan lebar celah ya...

Kasus celah bibir dan palatum, adalah kasus yang memiliki tingkat kesulitan lebih tinggi dalam hal perbaikan bila dibandingkan dengan kasus kecacatan lain yang disebabkan oleh cacat bawaan maupun dapatan lain. Karena ka...

Latar Belakang. Pasien dengan kelainan asimetri wajah termasuk diantarnya adalah pasien dengan celah bibir dan lelangit memerlukan analisis cefalometri postero-anterior. Tujuan Penelitian. Penelitian pendahuluan ini dila...