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Goldenhar syndrome

Goldenhar syndrome: a cause of secondary immunodeficiency?

Goldenhar syndrome: a cause of secondary immunodeficiency?

... Down syndrome, cleft palate, Townes and oral-facial-digital syndromes, and the Di George anomaly that are known to have a higher inci- dence of recurrent or persistent otitis ...Down syndrome, stenotic ear ...

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In vivo confocal microscopy in goldenhar syndrome: a case report

In vivo confocal microscopy in goldenhar syndrome: a case report

... Case presentation: A 15-year-old Caucasian female affected by Goldenhar Syndrome showed a left, infero- temporal, limbal neoformation, with extension to the left orbital region. Prior to surgical removal, ...

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Craniofacial abnormalities in goldenhar syndrome: a case report with review of the literature

Craniofacial abnormalities in goldenhar syndrome: a case report with review of the literature

... Goldenhar syndrome (oculo-auriculo-vertebral spectrum) is a rare congenital anomaly of unclear etiology and characterized by craniofacial anomalies such as hemifacial microsomia, auricular, ocular and ...

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Goldenhar Syndrome in a 6-Year-Old Patient: a Case Report and Review of Literature

Goldenhar Syndrome in a 6-Year-Old Patient: a Case Report and Review of Literature

... Goldenhar syndrome (GHS) is a complex syndrome characterized by relation of man- dibular hypoplasia, abnormality of the ear, ocular dermoid and vertebral disorders and hemi facial ...

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Management of Anesthesia in Goldenhar Syndrome: Case-Series Study

Management of Anesthesia in Goldenhar Syndrome: Case-Series Study

... Shukry et al. in 2005 reported the airway management of an 8-year old child with Goldenhar syndrome. He was a candidate for mandibular distraction surgery. He had a history of difficult tracheal intubation ...

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A Female Case of Goldenhar Syndrome with Mandibular Hypoplasia and Aural Involvement

A Female Case of Goldenhar Syndrome with Mandibular Hypoplasia and Aural Involvement

... Goldenhar syndrome (GS) is a poly-malformation syndrome, also defined as oculo-auricolo- vertebral dysplasia with hemifacial microsomia. It is a rare congenital defect involving first and second ...

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Goldenhar syndrome with blepharophimosis and limb deformities: a case report

Goldenhar syndrome with blepharophimosis and limb deformities: a case report

... with Goldenhar syndrome in association with blepharophimosis, ocular hypertelorism, hearing loss and limb deformities, underwent two operations and achieved a satisfactory ...with Goldenhar ...

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Goldenhar Syndrome with Occipital Meningoencephalocele: A Rare Case

Goldenhar Syndrome with Occipital Meningoencephalocele: A Rare Case

... Due to delay in growth and development of affected areas of child, conse- quences of Goldenhar Syndrome are more obvious as the child grows. In our case patient had preauricular tag, epibulbar dermoid, ...

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Applied Topics in Health Psychology

Applied Topics in Health Psychology

... 522 Index Golden Gurus language program 67 Goldenhar syndrome 244 Good Life Club GLC project 7 Good Sports program 327-9 accreditation leve1s 328 grief, benefit of companion animals 138 [r] ...

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Novel Technique for Placement of Laryngeal Mask Airway in Difficult Pediatric Airways

Novel Technique for Placement of Laryngeal Mask Airway in Difficult Pediatric Airways

... A total of 30 children with DA (11 girls and 19 boys) in the age range of 1.5 months to 10 years weighing 1.5 to 16 kg who were candidates for ocular surgery entered the study. Duration of surgical operation was 30 to 60 ...

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A Lebanese family with autosomal recessive oculo-auriculo-vertebral (OAV) spectrum and review of the literature: is OAV a genetically heterogeneous disorder

A Lebanese family with autosomal recessive oculo-auriculo-vertebral (OAV) spectrum and review of the literature: is OAV a genetically heterogeneous disorder

... anomalies. Goldenhar syndrome is a variant of this spectrum and is characterized by pre-auricular skin tags, microtia, facial asymmetry, ocular abnormalities, and vertebral anomalies of different sizes and ...

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The Fifth Phakomatosis – A Case Report

The Fifth Phakomatosis – A Case Report

... Based on the clinical, radiographic findings and FNAC report, a provisional diagnosis of multiple Odontogenic Keratocyts was given. This raised a suspicion of Gorlin-Goltz syndrome and thus the patient was ...

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Systemic Lupus Erythematosus: A Review

Systemic Lupus Erythematosus: A Review

... hypertension syndrome, characterized by an elevated intracranial pressure, papilledema, and headache with occasional abducens nerve paresis, absence of a space-occupying lesion or ventricular enlargement, and ...

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Relative safety of steroid sparing agents in frequently relapsing, steroid dependent and steroid resistant nephrotic syndrome in pediatric patients

Relative safety of steroid sparing agents in frequently relapsing, steroid dependent and steroid resistant nephrotic syndrome in pediatric patients

... nephrotic syndrome (FRNS), steroid-dependent nephrotic syndrome (SDNS) and steroid resistant nephrotic syndrome (SRNS) steroids are usually ...

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Significance of defecography and the role of rectocele in constipated patients

Significance of defecography and the role of rectocele in constipated patients

... Anorectal outlet obstruction is a form of chronic con- stipation in which pan-colonic transit time is normal but there is delayed transit in the rectosigmoid segment. Some of these patients have dilatation of the rectum ...

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The expanding spectrum of rare monogenic autoinflammatory diseases

The expanding spectrum of rare monogenic autoinflammatory diseases

... Blau syndrome, and Pyogenic sterile Arthritis, Pyoderma gangrenosum and Acne (PAPA) syndrome, have been extensively reviewed since the concept of autoinflammation was created in 1999 ...

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Extra Aneurysmal Flow Modification Following Pipeline Embolization Device Implantation: Focus on Regional Branches, Perforators, and the Parent Vessel

Extra Aneurysmal Flow Modification Following Pipeline Embolization Device Implantation: Focus on Regional Branches, Perforators, and the Parent Vessel

... RESULTS: Slow flow was observed in 13 of 68 (19.1%) side branches covered by the Pipeline Embolization Device. It was reported in all cases of anterior cerebral artery coverage, in 3/5 cases of M2-MCA coverage, and in ...

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... FIGURE 1. Typical presentation of posterior reversible encephalop- athy syndrome. Brain computerized tomography demonstrates areas of a white matter hypodensity affecting symmetrically: Frontal lobes (A), and ...

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Counselling people labelled with asperger syndrome

Counselling people labelled with asperger syndrome

... support a client with formulating practical strategies for managing breakdowns in communication. These might include identifying whom to go to for guidance or using a phrase to 'buy processing time', such as 'let me ...

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Mutiple keratocystic odontogenic tumors (KCOT) in a patient with Gorlin syndrome: a case report with late presentation and absence of skin manifestations

Mutiple keratocystic odontogenic tumors (KCOT) in a patient with Gorlin syndrome: a case report with late presentation and absence of skin manifestations

... KCOT occurring in Gorlin syndrome have a higher recurrence rate as compared to nonsyndromic soli- tary keratocysts [9]. This aggressive behavior may be explained by the presence of daughter and satellite cysts in ...

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