نتایج جستجو برای: ehlers danlos syndrome

تعداد نتایج: 622312  

Journal: :Gut 1969
P H Beighton J L Murdoch T Votteler

The gastrointestinal abnormalities encountered in 125 patients with the Ehlers-Danlos syndrome have been described. Spontaneous perforation of the intestine and massive gastrointestinal haemorrhage are uncommon but potentially lethal complications of the Ehlers-Danlos syndrome. Less dangerous abnormalities, such ;as external hernia, hiatus hernia, eventration of the diaphragm, intestinal divert...

Journal: :British journal of anaesthesia 1980
E Abouleish

The obstetric and anaesthetic problems of Ehlers-Danlos syndrome are discussed. A new unclassified type of the syndrome is described. The possibility of bleeding presents a serious challenge for both the obstetrician and the anaesthetist. A detailed medical history, including family history, are important in determining the method of anaesthesia since blood coagulation tests are usually normal....

2011
Mariam Rana Omer Aziz Sanjay Purkayastha Josephine Lloyd John Wolfe Paul Ziprin

INTRODUCTION Colonoscopic perforation is a rare but serious complication of colonoscopy. Factors known to increase the risk of perforation include colonic strictures, extensive diverticulosis, and friable tissues. We describe the case of a man who was found to have perforation of the sigmoid colon secondary to an undiagnosed connective tissue disorder (Ehlers-Danlos syndrome type IV) while unde...

Mahmoud Farhoudi Nasser Tayyebi Meybodi Vahid Mashayekhi Guyunlou Yalda Nahidi, Zari Javidi

Ehlers-Danlos syndrome (EDS) is a heterogenous group of inherited disorders of connective tissue characterized by fragility of the skin and blood vessels, hyperextensibility of the skin and joint hypermobility. Cutis laxa is characteized clinically by lax, pendulous skin and histologically by loss of elastic tissue in the dermis. There are some reports of coexistence of cutis laxa with ot...

2015
Paolo Ruggeri Salvatore Calcaterra Giuseppe Girbino

Ehlers-Danlos syndrome, characterized by hyperextensible skin, hypermobile joints, and fragile vessels, is the most common heritable disorder of connective tissue and has an estimated prevalence of 1 in 5000. Pulmonary involvement with signs of lung destruction (bullous emphysema) as first presentation is unusual. We report a case of monozygotic twins 37 years old men with occasional evidence o...

2016
Anna K. Ermarth John Pohl Brittany Esty Jessica K. Sempler John C. Carey Molly A. O’Gorman

We report the first observation of a patient with contgenital chylous ascites (CCA) and Ehlers-Danlos syndrome type VI due to primary lymphatic defect with additional vascular anomaly. CCA is a rare condition, and there is limited understanding of its pathophysiology and treatment options. We also review the patient's treatment course mitigated with octreotide and total parenteral nutritional s...

2015
Raimundo José Almeida de Oliveira Pinto Adaílton Araújo dos Santos Mablo de Castro Azevedo Saulo Sacramento Meira

Ehlers-Danlos syndrome is a rare clinical condition caused by a genetic change that results in the formation of structurally or functionally altered collagen. The clinical manifestations are varied, being the most obvious skin hypermotility and increased joint flexibility, although other systems - such as cardiovascular, respiratory and neurological - may also be affected. This paper presents t...

2013
Sophie Ronceray Juliette Miquel Antoine Lucas Gérald E. Piérard Trinh Hermanns-Lê Anne De Paepe Alain Dupuy

Ehlers-Danlos syndrome type VIII (EDS-VIII) is a very rare autosomal dominant disease characterized by early-onset periodontitis associated with features of Ehlers-Danlos syndrome. We report a 32-year-old man whose chronic leg ulcer led to the diagnosis of EDS-VIII. He had severe periodontitis with complete loss of permanent teeth and skin fragility with thin skin, atrophic scars, and brownish ...

Journal: :Internal medicine 2002
Takashi Nishida Shoichiro Ishihara Tatsumi Kaji Shingo Tajima Hajime Tanabe Kazuo Motoyoshi Keiko Kamakura

A 59-year-old man with abnormal vascular features (intracranial aneurysm, a cervical arteriovenous shunt, bilateral internal jugular vein occlusions, and left transverse sinus hypoplasia), as well as left optic atrophy was suspected to have familial polycystic kidney disease. The possibility of autosomal dominant polycystic kidney disease complicated by Ehlers-Danlos syndrome type IV due to the...

Journal: :Clinical Case Reports 2021

Ehlers-Danlos syndrome, specifically EDS4, can be a dangerous condition. Clinicians should aware of this when referring such patients for any interventional procedure. An MDT approach adopted to help plan perioperative treatment and care.

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید