نتایج جستجو برای: vomer agenesis

تعداد نتایج: 5340  

Journal: :Proceedings of the Royal Society of Medicine 1935

Journal: :Journal of radiology case reports 2013
David Besachio Edward Quigley Richard Orlandi Hugh Harnsberger Richard Wiggins

Myxomas of bone in the head and neck are rare tumors. We present a 68 year old female with pain and epistaxis who was found to have the first reported case of a myxoma arising within the vomer bone. Some atypical magnetic resonance imaging features are described, however, myxoma imaging features are often non-specific and typically evoke a benign differential diagnosis. Surgical excision is the...

Journal: :Zootaxa 2013
Yuki Nagano Mark A McGrouther Mamoru Yabe

A new species of hoplichthyid, Hoplichthys imamurai, is described on basis of three specimens (128.9-143.6 mm SL) collected from northern Western Australia. It is clearly distinguished from its congeners by the following combination of characters: short preoptic snout (31.2-32.7% HL); vomer without teeth; long, thin, gill rakers; low first dorsal fin, its ad-pressed tips not reaching origin of ...

  Pulmonary agenesis is a rare congenital anomaly in which there is absence of pulmonary parenchyma as well as its bold vessels. It is an unusual cause of respiratory distress in newborn. Unilateral agenesis of lung is often associated with other congenital anomalies. The condition may lead to diagnostic difficulties.   Right pulmonary agenesis has poor prognosis. Here we present a case of fem...

Congenital agenesis of lumbar vertebrae was diagnosed in a day-old female lamb based on radiology and clinical examinations. There was no neurological deficit in hindlimb and forelimb associated with standing disability. Radiography of the abdominal region revealed absence of lumbar vertebrae. Necropsy confirmed clinical and radiographic results. No other anomaly or agenesis was seen macroscopi...

Journal: :The Journal of craniofacial surgery 2009
Peter J Taub Joshua A Lampert Lester Silver Alex Greenberg

Patients with clefts of the lip and palate commonly develop maxillary hypoplasia. In addition to orthognathic surgery, augmentation of the anterior maxilla may be necessary in these patients to restore symmetry to the nasomaxillary complex. Bone graft may be obtained from numerous sites. All require a separate incision at the donor site and may result in additional morbidity.The authors describ...

Hekmatfar, Somayeh, Jafari, Karim, Rezayi, Amir, Samadi, Vahid,

Introduction: This study aimed to investigate the relationship between the prevalence of dental anomalies and hypodontia. Materials and Methods: In this retrospective study, the panoramic radiographs of 101 cases with tooth agenesis (except for the third molar) were studied and compared with [Pn1] those of a non-agenesis control group of 182 subjects. The subjects were within the age range of ...

2015
Marco FERRARI Manfred TSCHABITSCHER Rita REZZANI Luigi F. RODELLA Luigi F. Rodella

Introduction Middle nasal turbinate (concha) is one of three or four lateralto-medial extroflexions of the lateral nasal wall: they are the inferior turbinate, whose bony skeleton is an independent bone, and middle, superior and sometime supreme turbinates, whose bony structures are part of the ethmoid bone. Embryogenesis of the last three turbinates is a process induced by active intramural pn...

Hekmatfar, Somayeh, Hoseini, Saleh, Jafari, Karim, Mikaili, Hesam,

Introduction: Hypodontia is one of the most common developmental anomalies. This study aimed to evaluate the variations of radiographic dental development in a group of Iranian children with dental agenesis. Materials and Methods: This study evaluated 1230 Orthopantomographs (OPGs) for agenesis of permanent teeth obtained from the patients aged between 8 and 18 years. Then the difference betwe...

Delshad, Salaheddin, Mardi, Parham,

Introduction: Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome is a rare disorder in women which identified as agenesis of vagina and hypoplasia or agenesis of uterine. Case presentation: in this study, two female cases (17, and 19 years old) diagnosed with MRKH (first one type 2, and second one type 1) are described. Both patients were presented with amenorrhea, and absence of vagina orifice. On...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید