نتایج جستجو برای: facial anomaly

تعداد نتایج: 98946  

Journal: :iranian journal of otorhinolaryngology 0
shahin abdollahi fakhim department of otolaryngology head and neck surgery, tabriz university of medical sciences, tabriz, iran. nikzad shahidi department of otolaryngology head and neck surgery, tabriz university of medical sciences, tabriz, iran.

introduction: tessier facial cleft is among the rarest facial clefts reported in literatures and there are many issues arguing about its multidisciplinary repairing techniques. tessier number 4 and 5 are extremely rare facial anomalies. there are few literatures describing these clefts and their surgical modalities. number 5 tessier cleft begins medial to oral commissure in the upper lip and ex...

Journal: :iranian journal of otorhinolaryngology 0
shahin abdollahi fakhim department of otorhinolaryngology head and neck surgery, tabriz university of medical sciences, tabriz, iran. nikzad shahidi department of otorhinolaryngology head and neck surgery, tabriz university of medical sciences, tabriz, iran. alireza lotfi department of otorhinolaryngology head and neck surgery, tabriz university of medical sciences, tabriz, iran.

introduction: orofacial clefts are among the most common congenital anomalies. patients presenting with orofacial clefts often require surgery or other complex procedures. a cleft lip or palate can be a single anomaly or a part of multiple congenital anomalies. the reported prevalence of cleft disease and associated anomalies varies widely across the literature, and is dependent on the diagnost...

Nikzad Shahidi, Shahin Abdollahi Fakhim

Introduction: Tessier facial cleft is among the rarest facial clefts reported in literatures and there are many issues arguing about its multidisciplinary repairing techniques. Tessier number 4 and 5 are extremely rare facial anomalies. There are few literatures describing these clefts and their surgical modalities. Number 5 Tessier cleft begins medial to oral commissure in the upper lip and ex...

A. Fazel A. Niazi A. Omidi, M. Gharavian N. Sharifi

Bilateral femoral agenesis is a rare anomaly.  To the best of our knowledge, only three cases of simple congenital anomaly and three cases associated with femoral facial syndrome have been reported.  Here, we describe a simple form of bilateral femoral agenesis observed in one of the 2 dead fetuses delivered after termination of a 24-week twin pregnancy of a normal mother.  Post-mortem x-ray ex...

Journal: :iranian journal of medical sciences 0
a. omidi n. sharifi a. fazel a. niazi m. gharavian

bilateral femoral agenesis is a rare anomaly.  to the best of our knowledge, only three cases of simple congenital anomaly and three cases associated with femoral facial syndrome have been reported.  here, we describe a simple form of bilateral femoral agenesis observed in one of the 2 dead fetuses delivered after termination of a 24-week twin pregnancy of a normal mother.  post-mortem x-ray ex...

Journal: :Kathmandu University medical journal 2015
S Das I P Tuli

Numerous anomalies and variations of facial nerve anatomy leading to iatrogenic injury are described. However, there are no reports of facial nerve dehiscence near its second genu causing a hump and obstructing middle ear ventilation pathway, as found in our case. This particular anomaly of facial nerve is being reported to highlight its uniqueness and that a dehiscent facial nerve may be a rar...

Abdollahimohammad, Abdolghani , Amirshahi, Mehrbanu , Kerami, Azam , Mansoorifar, Leila , Mirshekari, Fatemeh , Mirshekari, Leila , Mirshekari, Marzeeh , Naroei, Fereshteh , Salehi, Ashraf , Sanagoo, Akram ,

Holoprosencephaly (HPE) is a rare congenital brain malformation associated with multiple midline facial defects. This anomaly is resulted from the failure of diverticulation and cleavage of primitive prosencephalon during weeks 4-8 of gestation. HPE is the most common forebrain developmental anomaly in human with the incidence rate of 0.49-1.2 cases per 10,000-20,000 term births. In this study,...

Majtaba adineh Maryam saeidi, Reza saeidi,

Cornelia de Lange syndrome (CdLS) is an uncommon multiple congenital anomaly with unknown cause and recurrent risk and may be the result of an inheritance metabolic error. In classical form of the syndrome there is a recognizable facial appearance at birth although in children with mild disease this may be less obvious at birth but become more noticeable over the first three years of life. In t...

Introduction: Orofacial clefts are among the most common congenital anomalies. Patients presenting with orofacial clefts often require surgery or other complex procedures. A cleft lip or palate can be a single anomaly or a part of multiple congenital anomalies. The reported prevalence of cleft disease and associated anomalies varies widely across the literature, and is dependent on the diagnost...

2016
Dong Hoon Lee Tae Mi Yoon Joon Kyoo Lee Sang Chul Lim

The branching pattern of the facial nerve varies among individuals. These variations increase the risk of facial nerve injury during parotid surgery. We report a new variation of the facial nerve and an unusual relationship with the retromandibular vein during parotid surgery.Clinicians should recognize this facial anomaly and the unusual relationship with the retromandibular vein to avoid inju...

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