نتایج جستجو برای: constrictive amenorrhea syndactyly

تعداد نتایج: 5137  

2005
C. SIDNEY BURWELL

SIXTY-EIGHT patients with constrictive pericarditis were studied by this laboratory in a 30-year period. During this time 14 patients were encountered whose findings suggested constrictive pericarditis but who showed an abnormal myocardium at operation or autopsy. Two of these patients had both constrictive pericarditis and myocardial fibrosis, each of the other 12 had a no: mal pericardium. Th...

Journal: :Urology journal 2008
Abolhassan Seyedzadeh Farshid Kompani Ebrahim Esmailie Sara Samadzadeh Bohaire Farshchi

Received November 2007 Accepted March 2008 INTRODUCTION In 1964, Pfeiffer described an acrocephalosyndactyly syndrome consisting of bicoronal craniosynostosis, midface hypoplasia, broad thumbs, broad big toes, and partial and variable soft-tissue syndactyly of the hands and feet.(1) Autosomal dominant inheritance with complete penetrance is the main characteristic despite variable expressivity ...

2016
Tuba Tulay Koca

Apert syndrome is the rare acrocephalosyndactyly syndrome type 1, characterized by craniosynostosis, severe syndactyly of hands and feet, and dysmorphic facial features. It demonstrates autosomal dominant inheritance assigned to mutations in the fibroblast growth factor receptor gene. Presently described is case of a 19-year-old female patient diagnosed on physical examination with Apert syndro...

Journal: :The Eurasian journal of medicine 2008
Canan Atalay Nazim Dogan Şahin Yüksek Ali Fuat Erdem

Apert syndrome is a type of acrocephalosyndactilia that consists of craniofacial synostosis, midface hypoplasia and syndactyly, with an autosomal dominant inheritance pattern. During anesthesia, difficult intubation and ventilation may be observed because of abnormal airways. In one of our patients, visceral anomalies, such as esophageal stricture and post-strictural dilatation, may cause respi...

2014
Niraj Kumar Shubhangi Arora Ashish Bindra Keshav Goyal

Apert syndrome is an autosomal dominant disease characterized by craniosynostosis, midface hypoplasia and syndactyly. In general, patients present in early childhood for craniofacial reconstruction surgery. Anesthetic implications include difficult airway, airway hyper-reactivity; however, possibility of raised intracranial pressure especially when operating for craniosynostosis and associated ...

Journal: :Journal of the American College of Cardiology 2011

2017
Gauranga Majumdar Surendra Kumar Agarwal Shantanu Pande Bipin Chandra Prabhat Tewari

We here report a successful midterm outcome following combined off-pump radical pericardiectomy and coronary artery bypass surgery (CABG) in a 65-year-old male patient who was suffering from chronic constrictive calcified tubercular pericarditis with coronary artery disease. Simultaneous off-pump CABG and radical pericardiectomy for nonsurgical constrictive pericarditis is reported very rarely ...

2011
Amal Lachhab Nawal Doghmi Abdellah Zouhairi Anis Seghrouchni Fouad Amal Wahid Abdellatif Boulahya Wajih Maazouzi Youssef Elfakir Omar Taoussi Rachida Amri Loubna Belhaj Laila Haddour Rhizlane Cherradi Latifa Oukerraj Mohamed Cherti

BACKGROUND The diagnosis of constrictive pericarditis continues to be a clinical challenge. Magnetic resonance imaging provides excellent visualization of the pericardium. The aim of our study is to clarify the contribution of this non invasive exploration in the diagnosis of constrictive pericarditis in our center. METHODS we conducted a prospective study over a period of two years, since 20...

Journal: :International journal of clinical and experimental medicine 2014
Shi-Min Yuan

Massive ascites of unknown origin is an uncommon condition, which represent a diagnostic challenge. Patients with delayed diagnosis and treatment may have a poor prognosis. A 22-year-old female was referred to this hospital due to a 4-year progressive abdominal distension with massive ascites of unknown origin. By thorough investigations, she was eventually diagnosed as chronic calcified constr...

Journal: :Proceedings of the Royal Society of Medicine 1942

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