[PDF] Top 20 case report: Werner’s Syndrome

... nans görüntüleme (MRG) istendi. Sonuç normal olarak geldi. Nörologların önerisiyle çekilen beyin MRG da bilateral optik sinir kılıfı etrafında sıvı artışı ve bilateral kaudat nükleusta ve globus palli- duslarda T1A ... See full document

... rações do esôfago cervical apresenta baixa morbidade, podendo oferecer aos pacientes a preservação do órgão em um único tempo cirúrgico, sendo o tratamento de es- colha em muitos Serviço[r] ... See full document

... protein S, and activated protein C resistance have been observed, suggesting a possible biological link between the vasculopathy and a primary coagulopathy in SS (3,8) ... See full document

... the case of a two-year-old girl with fe- ver, bone pain and weight loss, whose investigation and follow-up led to the diagnosis of ...only case of GS described in the Portuguese ... See full document

... outlet syndrome (TOS) is defined as a set of symptoms caused by the compression of the bra- chial plexus and subclavian vessels in the thoracic outlet ...a case of a young woman with pain in the left ... See full document

... We report a case of 15 year old female, age of 5 years, presented to us with diabetic the ...be s than 3 rd percentile) and weight was 27 kg (le und face and protuberant ...Mauriac syndrome is ... See full document

... Alport syndrome can be confirmed or excluded in the majority of cases by the performance of a renal biopsy with analysis of type IV collagen expression in the ... See full document

... associated with presence of scaly lesions on 2. Subramaniam P, Mathew S, Gupta K K. the hands and toes for the last 9 years. Early Papillon-Lefevre Syndrome: A case report. J exfoliation of ... See full document

... Perlman syndrome, Beckwith –Wiedemann syndrome, VACTERL association, Pfeiffer syndrome type 3, and MMIHS suggesting the possi- bility of a common pathogenesis ... See full document

... autoimmune syndrome is defined as multiple endocrine gland insufficiencies accompanied by autoimmune diseas- es of the endocrine and nonendocrine ...a case of nontuberculosis adrenal gland dysfunction with ... See full document

... this syndrome has been solely focused on addressing sensorineural hearing loss by cochlear implants if detected at an early age, the occurence of reduced vision, problems related to the ocular appearance, as well ... See full document

... Lange´s syndrome is a genetic anomaly, described and published by Cornelia Catharina of Lange in 1933, however, their aspects were described previously by Winfried Robert Clemens Brechmann in 1916, that’s ... See full document

... Case report: We report the case of a 24-h-old newborn with Goldenhar’s syndrome. He had esophageal atresia with distal tracheoesophageal fistula. It was decided that an emergency ... See full document

... Abstract: Lichen nitidus is a disease of unknown etiology, characterized by flesh-colored, shiny papules of 1-2 mm and generally asymptomatic or with mild pruritus. The most common sites of occurrence are genitalia, ... See full document

... The prognosis of the VAHS is mainly based in the severity and duration of the cytopenias. Long-term neutropenia increases the risk of severe infections, including gram-positive bacteria, such as S. aureus. ... See full document

... se s la te ral nom de vi ja ci jom, što iza zi va gla vo- bo qu ili bo lo ve is pod oka, sle po oè no i u pre de lu ma sto id nog na stav ka s iste stra ... See full document

... Herlyn-Werner-Wunderlich syndrome (HWWS), also known as obstructed hemivagina and ipsilateral renal anomaly (OH- VIRA) syndrome was first described in ...the syndrome often appears as a single ... See full document

... On the sixth day of illness, the patient’s clinical condition deteriorated further and she presented psychomotor agitation, arterial hypotension and acute respiratory failure. The patient was referred to the intensive ... See full document

... cialties, has potential to change the course of this severe pa- thology. Also, its characteristics can precipitate se veral other medical conditions as described in this case, and a multi-pro- fessional healthcare ... See full document

... Herlyn-Werner-Wunderlich syndrome (HWWS), characterized by uterus didelphys, obstructed hemivagina, and ipsilateral renal agenesis, is a rare combined Mullerian and mesonephric duct ... See full document