نتایج جستجو برای: mandibular limb hypogenesis syndrome

تعداد نتایج: 708065  

Journal: :Journal of clinical and diagnostic research : JCDR 2015
Pradkhshana Vijay Nilesh Pardhe Vsb Sunil Manas Bajpai Neha Chhibber

Condylar aplasia which means "failure of development" is a rare condition and can be unilateral or bilateral. Mandibular condylar Aplasia without any association with syndrome is extremely rare. Temporomandibular joint (TMJ) ankylosis results from trauma, infection and inadequate surgical treatment of the condylar area. Congenital cases are very rare. We report case of congenital unilateral apl...

2018
Igor-Moreira Hazboun Thiago-Pires Brito Vanessa-Gonçalves Silva Carlos-Eduardo-Monteiro Zappelini Leopoldo-Nizam Pfeilsticker

Introduction SAPHO syndrome is defined as the association of a group of rare sterile osteoarticular disorders and inflammatory skin diseases whose etiology, although not yet determined, probably involves genetic, immunological and infectious mechanisms. The recurrent multifocal osteomyelitis, an inflammatory disease, can be associated with this syndrome even as a single event. Case Report A c...

2017
Yu Kamata Tomohiro Yamada Tomoki Sumida Hiroyuki Nakano Goro Sugiyama Azusa Nakashima Yoshihide Mori

SAPHO syndrome is a chronic disease of unknown etiology, which is characterized by synovitis, acne, pustulosis, hyperostosis, and osteitis, however, pediatric osteomyelitis of the jawbone is rarely reported. We present a report of pediatric nonbacterial osteomyelitis of the mandible associated with SAPHO syndrome. A seven-year-old girl presented complaining of pain in, and swelling of, the righ...

Journal: :Journal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery 2009
Elena Di Palma Giulio Gasparini Sandro Pelo Gianluca M Tartaglia Claudio Chimenti

AIM To evaluate left and right masseter and anterior temporalis muscle activity in patients before and after orthognathic surgery. PATIENTS Nineteen patients were enrolled, 9 males and 10 females, aged 17-34 years. Four patients were suffering from a prognathic syndrome (skeletal class II with mandibular retrusion) and were candidates for surgical correction involving a mandibular Bilateral S...

Journal: :international journal of pediatrics 0
nemat bilan pediatric health research center , tabriz university of medical sciences, tabriz iran. mohammad barzegar pediatric health research center , tabriz university of medical sciences, tabriz iran. parinaz habibi pediatric health research center , tabriz university of medical sciences, tabriz iran.

introduction:guillain-barre syndrome(gbs) is the most common cause of acute flaccid paralysis. respiratory failure is the most serious short-term complication of gbs and invasive mechanical ventilation is required in 30% of patients.moreover,60% of those who are intubated develop major complications including pnemonia,sepsis,gi bleeding and pulmonary embolism. thus respiratory failure predictio...

Journal: :International journal of applied dental sciences 2023

Klippel-Feil Syndrome is a complex condition due to aberrant fusion of two or more cervical vertebrae characterised by short neck, low hairline, facial asymmetry and limited neck movement. Mandibular hypoplasia, submucous cleft, congenitally missing teeth, asymmetries mouth breathing are frequently observed in patients with Syndrome. Management symptomatic supportive which necessitates multidis...

Journal: :The Journal of the Association of Physicians of India 2013
Ravikar Ralph Anugrah Chrispa

a 48 year old Indian male presented with a painless swelling of the right upper limb since birth associated with an overlying discolouration involving the right chest wall. at presentation, he complained of increased sweating and a tingling sensation over the involved limb. Clinical examination revealed a port wine stain over the right upper limb and hemithorax extending from the base of the ne...

Journal: :Journal of Bangladesh College of Physicians and Surgeons 2016

Journal: :American journal of human genetics 2006
C G Woods S Stricker P Seemann R Stern J Cox E Sherridan E Roberts K Springell S Scott G Karbani S M Sharif C Toomes J Bond D Kumar L Al-Gazali S Mundlos

Fuhrmann syndrome and the Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome are considered to be distinct limb-malformation disorders characterized by various degrees of limb aplasia/hypoplasia and joint dysplasia in humans. In families with these syndromes, we found homozygous missense mutations in the dorsoventral-patterning gene WNT7A and confirmed their functional significance in retrov...

2014
Christine SAUVÉ Thomas WOJCIK Joël FERRI

Orthodontists and maxillo-facial surgeons are very aware of the different therapeutic options for the correction of maxillary transverse deficiencies. But what about mandibular transverse deficiencies? A number of dentofacial orthopedic mandibular expansion techniques have been suggested, but they often have a tendency to relapse. Symphyseal distraction is the easiest solution for the correctio...

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