poisoning remains a major cause of hospital admission into the emergency department and intensive care unit. proper diagnosis is the cornerstone for optimal management of poisoned patients. since the definitive analytical confirmation of the nature of the toxicant involved in the poisoning cannot be rapidly obtained in the majority of healthcare facilities, diagnosis relies on the medical histo...

klinefelter syndrome includes a group of chromosomal disorders with at least one  additional  x  chromosome  in  male  karyotype  (46,xy).  up  to  now, different dental manifestations such as taurodontism, congenital absence of permanent teeth, shovel incisors, occlusal anomalies and increased permanent tooth size have been reported. a case of klinefelter syndrome with very rare dental feature...

EB is a prototypic and heterogeneous group of inherited bullous disorders characterized by detachment the epithelium following minimal mechanical trauma. The phenotypic spectrum broad, with persistent blistering, inflammation, delayed re-epithelialization, dysfunctional wound healing often infection, leading to disability and, in most severe cases, death. classified into four subtypes: simplex ...

conclusions adherence to the meddiet, according to mds and sofi-mds, may not predict mets components and mets incidence after 3 years of follow-up in iranian adult populations. results after adjusting for potential confounders, neither higher mds nor higher sofi-mds were significantly associated with the mean values of mets components and the risk of metabolic abnormalities incidence after 3 ye...

The lingual frenum is a mucosal fold that connects the bottom of the body of the tongue to the floor of the mouth and to the mandibular bone. Ankyloglossia results when the frenum is thick and very tight and/or its place of insertion limits the mobility of the tongue. If the anomaly is relatively severe and generates mechanical limitations and functional challenges, surgical reduction of the fr...

introduction: cervical rib is relatively uncommon congenital abnormality that originates from the seventh cervical vertebrae and rarely from the sixth vertebrae. the purpose of this paper is to consider that this abnormal condition is an important cause of neurovascular compression at the thoracic outlet. methods: in this study all patients who were referred to radiology department of isfahan h...

introduction women with mosaic turner syndrome (ts) bearing the presence of y chromosome material or with complete androgen insensitivity syndrome (cais) is at risk of gonadal malignancy. two patients with characteristic features of these uncommon disorders are reported, and the surgical techniques of laparoscopic gonadectomy are reviewed and discussed. the aim of the present study is to report...