JAK-STAT signaling: molecular mechanism and targeted treatment in dento-maxillofacial abnormalities [PDF]
International Journal of Oral ScienceDento-maxillofacial abnormalities are highly prevalent and arise as a result of a variety of etiological factors, presenting substantial challenges to treatment.
Lingyong Jiang
exaly +4 more sources
Intraoral and maxillofacial abnormalities in patients with autosomal dominant hyper-IgE syndrome [PDF]
Central-European Journal of Immunology, 2023 Autosomal dominant hyper-IgE syndrome (AD-HIES) is an inborn error of immunity (IEI) caused by a dominant-negative mutation in the signal transducer and activator of transcription 3 (STAT 3). This disease is characterized by chronic eczematoid dermatitis,
Melinda Erdos
exaly +4 more sources
Editorial: Stem cell therapy in dentistry and oral and maxillofacial abnormalities [PDF]
Frontiers in Cell and Developmental BiologyIlya Klabukov +2 more
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Clinical value of maxillofacial characteristics in Turner syndrome patients [PDF]
Jichu yixue yu linchuang, 2020 Turner syndrome has characteristic maxillofacial abnormalities associated with a variety of diseases, including conductive hearing loss, feeding difficulties, sleep apnea, and vocal abnormalities.
LIANG Si-yu, CHEN Shi, WANG Shi-rui, PAN Zhou-xian, ZHU Jia-wei, ZHU Hui-juan, PAN Hui
doaj +1 more source
Surface Electromyography as a Method for Diagnosing Muscle Function in Patients with Congenital Maxillofacial Abnormalities [PDF]
Journal of Healthcare Engineering, 2020 Liliana Szyszka-Sommerfeld +2 more
exaly +2 more sources
Maxillofacial 3D Imaging in Cleidocranial Dysplasia: A Case Report and Literature Review [PDF]
Journal of Kerman University of Medical Sciences, 2022 Cleidocranial dysplasia (CCD) is an inherited autosomal dominant disorder affecting the skeletal and craniofacial structures, exhibiting distinct maxillofacial abnormalities.
Mohamed Faizal Asan +4 more
doaj +1 more source
Parry Romberg syndrome with en coup de sabre: A report of a rare case [PDF]
Acta Stomatologica Naissi, 2021 The basis of the problem: Parry Romberg syndrome (PRS) is a rare developmental disorder manifesting as a slow and progressive atrophy of the face which is often unilateral, hence also termed as rpogressivehemifacial atrophy. The extent of the atrophy may
Faizal Asan Mohamed +4 more
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Acta Scientiarum. Health Sciences, 2012 Regional odontodysplasia is an uncommon, nonhereditary developmental dental disorder of unknown etiology, which should be early detected. This paper compares a regional odontodysplasia case with the clinical and radiographic characteristics reported in ...
Saulo André de Andrade Lima +5 more
doaj +3 more sources
Staged Nasal Reconstruction Using a Forehead Flap and Rib Bone and Cartilage Graft in a Binder Syndrome Patient: A Case Report [PDF]
Archives of Aesthetic Plastic Surgery, 2018 Binder syndrome is a rare maxillofacial abnormality. Yet, once presented, it often needs to be addressed surgically. To suit this purpose, various surgical techniques have been developed.
Jae-Woo Heo, Ung Sik Jin
doaj +1 more source
Prosthetic rehabilitation of a patient underwent hemimaxillectomy
Fogorvosi Szemle, 2023 Two options are available for the treatment of oronasal or oroantral fistulas caused by traumatic or resective surgery: reconstructive surgery and reconstructive prosthetic care. However, the choice between these options is often controversial: it is not
János König +3 more
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