Home

Spondylitis and ehlers danlos

EDS (hyper mobility?) and Ankylosing Spondylitis - Ehlers

Welcome to our site! I was diagnosed with Ankylosing Spondylitis when I was 37 (I'm now 42). I have the HLA-B27 marker, and damaged SI joints. I took Humira, and then Humira with Methotrexate for a while, with very little relief in pain symptoms. She sent me to a geneticist, who diagnosed me with Ehlers-danlos syndrome. They think I do NOT. A lot of the time, those who are in need of help have become isolated from peers, friends, family, you name it. Living with ankylosing spondylitis and Ehlers-Danlos syndrome has left friends fearful of contact, of hugs, of conversation and of sharing experiences in their day-to-day lives. Last year I was at a low point Psoriatic Arthritis, Ankylosing Spondylitis, Dermatomyositis, Polyarteritis Nodosa, and many others. •Ehlers-Danlos Syndrome occurs in tandem with comorbid conditions and modifiable or unmodifiable factors, all combining uniquely to affect each individual as a whole

Isolation of Living With Ankylosing Spondylitis, Ehlers

Jen970. June 4, 2015 at 11:48 am. Report. I've had surgery for herniation of L5-S1, constant pain in the sacroiliac area L>R, stiffness when I first get out of bed or stand after sitting for prolonged periods, chronic pain in mid-thoracic and have needed a fusion of C5-6, C6-7 for herniated discs and bone spurs Diagnosis: Ankylosing Spondylitis, Ehlers Danlos Syndrome, Fibromyalgia, and many additional comorbid diseases. This post contains affiliate links, which means I receive a small commission, at no extra cost to you, if you make a purchase using these links. Please read my disclosure for more information Ehlers-Danlos Syndrome (EDS) is a heterogeneous group of congenital connective tissue disorders thought to be caused by mutations in genes coding for collagen proteins (i.e. COL3A, COL5A. Since the new, much tighter criteria for the most common form of Ehlers-Danlos syndrome, hypermobile EDS now known as hEDS but especially ankylosing spondylitis (my dad and 2 aunts had this, and I have the factor for it) or multiple sclerosis As I've mentioned numerous times throughout this blog, people with a form of Ehlers-Danlos Syndrome or Hypermobility Spectrum Disorders seriously win the bad health lottery when it comes to comorbidities, or conditions you have along with a primary condition. (Aka co-occurring conditions in England I think.

The hypermobile type of Ehlers-Danlos Syndrome (hEDS) is the dominant form of EDS. A subpopulation of hEDS patients have been found to have MCAD (more often MCAS than SM). Several reports have described of co-morbid clinical manifestations in patients with CTDs,. Ehlers-Danlos Syndrome(s) involve a genetic mutation of one or more of our collagen proteins, at a cellular level. There are currently thirteen known subtypes, each involving a different mutation and varying degrees of symptoms, but all symptoms can cross over from one subtype to the next Ehlers-Danlos Syndrome. These rare, inherited disorders cause overly flexible joints and loose, fragile skin. Ehlers-Danlos syndrome (EDS) is a collection of genetic disorders that affect connective tissue. People who have EDS have problems with their collagen, a protein that adds strength and elasticity to connective tissue The term Ehlers-Danlos Syndrome (EDS) refers to a group of inherited connective tissue disorders. In many subtypes the genetic basis is now known. The skin, joints, blood vessels and hollow organs can all be affected with consequences varying from mild features to severe life threatening events. Ankylosing Spondylitis is an immune.

Your sacroiliac (SI) joints are the meeting point of your spine and pelvis. These joints can become unstable and painful for several reasons—and one cause is a rare genetic condition called Ehlers-Danlos syndrome (EDS). This article describes the relationship between EDS and SI joint dysfunction Ehlers-Danlos syndrome hypermobility type is associated with rheumatic diseases Sci Rep. 2017 Jan 4 ankylosing spondylitis, rheumatoid arthritis, fibromyalgia) than those with NWU or LWU. In conclusion, HEDS is associated with complicated rheumatological conditions, which are uncovered by comprehensive workup. These conditions require. The pain of being misunderstood, disbelieved, criticised - by former friends, colleagues, society, loved ones. The pain of being dismissed and invalidated by medical professionals until 'evidence' appears in blood tests, on x-rays, or a scan. We think of medical conditions as having a beginning, middle and end like Ehlers-Danlos disease, and Marfan's syndrome. Familial occurrence of intracranial aneurysms has also been reported2. Ankylosing spondylitis (AS) is a potentially disabling form of seronegative spondyloarthropathies. The major etiologic factor of AS is genetic predisposition, HLA-B27 being the most important. Both familial and sporadic A

Ankylosing Spondylitis & EDS Type 3 Diagnosis - Ehlers

Ehlers-Danlos Syndrome (EDS) is a group of genetic disorders of the connective tissue. Ehlers-Danlos Syndrome is a constellation of many different disorders, all sharing to some degree a defect in a patient's connective tissue that makes that tissue fragile and stretchy. This may result in complications ranging from increased bruising, loose joints, chronic pain, and some serious medical. There are numerous ocular complications of Ehlers Danlos Syndrome. It is important to understand which symptoms may be indicative of an urgent condition and which are merely annoying. Additionally, it can be difficult to know when a symptom is Ehlers Danlos Syndrome related or is an indication of a non-EDS condition Pseudoxanthoma elasticum (PXE) is a genetic systemic disorder, the hallmark of which is dystrophic mineralization of elastic tissue of the skin, retina, and arteries. PXE is caused by mutations in the gene that codes for the membrane transport protein ABCC6 (MRP6). Recent experiments on a PXE knockout mouse suggest that a circulating metabolite. Ehlers-Danlos Syndrome and Postural Tachycardia Syndrome: A relationship study. J Neurol Sci. 2014 Mar 11. pii: S0022-510X(14)00145-2. 29. Shibao C, Arzubiaga C, Roberts J, Raj S, Black B, Harris P, Biaggioni I. Hyperadrenergic Postural Tachycardia Syndrome in Mast Cell Activation Disorders. Hypertension. 2005; 45: 385-390. 30 Ehlers-Danlos syndrome (EDS) is the name given to a diverse group of inherited connective tissue disorders involving a genetic defect in collagen. Ehlers-Danlos syndrome, characterized by joint.

The sclera is the white layer of your eye and is made of

Surviving Together: Ankylosing Spondyliti

This question was answered during the episode of Spine Time called Ehlers-Danlos Syndrome: What is it and how is it treated? A video of that episode, held on August 19, 2020, is available here on YouTube. To sign up for future episodes of Spine Time, where you can ask questions of our spine specialists, subscribe here Ankylosing Spondylitis; Ehlers Danlos Syndrome; Crohn's Disease; Ulcerative Colitis; Rheumatoid Arthritis; Systemic Lupus Erythematosus (SLE/Lupus) this page is undergoing renovation and will be back online in february 2019 I've got 2 rare diseases (that have been identified so far), the 1st is called Ehlers Danlos Syndrome Hypermobility Type and the 2nd is called Ankylosing Spondylitis. Fun, huh? The 1st time I remember chronic pain being an issue was when I was around 13 years old. I went to the Dr's who referred me to a Rheumatologist In a study published in Rheumatology, researchers have described, in detail, the natural history of complaints and disabilities experienced by children diagnosed with joint hypermobility syndrome (JHS)/Ehlers-Danlos-hypermobility type (EDS-HT), and identified the constructs that underlie their clinically functional decline.. The JHS/EDS-HT phenotype generally consists of widespread arthralgia.

Ankylosing spondylitis is an uncommon form of arthritis, 1 a subcategory of rheumatoid arthritis, an autoimmune condition causing inflammation of the joints. Ankylosing refers to the stiffening or fusing of the joints, and spondylitis means irritation of the spine, so AS features spinal joint inflammation that can lead to bone. Pain found in EDS-H / JHS is unusual in the medical world because it is one of the few conditions causing both chronic and acute pain and because (except after dislocations etc.) it is notably pain without the inflammatory component of other rheumatological diseases. 'Joint Hypermobility Syndrome is the most frequent cause of musculo-skeletal. Ehlers-Danlos Syndrome (EDS) is a complex disorder and shares overlapping symptoms with other connective-tissue disorders, as well as other common conditions. In addition, there are 13 types of EDS alone - with varying treatments. If EDS is suspected, an early confirmed diagnosis is imperative to keep the condition from getting worse. Therefore, a patient will want to seek out a world-class.

Posts about Ehlers Danlos written by BeingCharis. About Charis. Unstoppable, award-winning advocate since 2013, Charis is a professionally disabled writer, speaker and model living with Ankylosing Spondylitis (AS), Major Depressive Disorder, Anxiety and Post-Traumatic Stress Disorder Ehlers-Danlos Syndrome is a group of genetic conditions that affect the connective tissue which provide strength and support to the structures in the body, according to the Mayo Clinic. Depending on the sub-type, symptoms may include very flexible joints, fragile skin, and bruising easily. In more severe cases or sub-types, veins and arteries. Ehlers-Danlos syndrome, hypermobility type, constituting a phenotypic continuum with or, perhaps, corresponding to the joint hypermobility syndrome (JHS/EDS-HT), is likely the most common, though the least recognized, heritable connective tissue disorder. Known for decades as a hereditary condition with predominant rheumatologic manifestations, it is now emerging as a multisystemic disorder. Ehlers-Danlos National Foundation Website. Community and Charitable Organizations: The ILC Foundation is a Canadian community and charitable organization specializing in awareness, education, advocacy and client support for children, adolescents and teens

Ehlers-Danlos syndrome hypermobility type is associated

Spondylitis may affect the low back, chest, and/or the neck. In the cervical spine, limitation of motion is a primary manifestation of neck involvement. The activity of skin and nail disease does not necessarily correlate with joint or spine involvement Ankylosing Spondylitis. Scenario: A 38-year-old male presents with complaints of low back pain with insidious onset and duration of over 3 months. He reports that his neck is also stiff, and driving a car has been difficult. He works for a company that provides computer technical support to many local businesses and needs to drive for his work Learn about ankylosing spondylitis including symptoms, diagnosis, treatment, patient stories, & more from an ankylosing spondylitis community perspective. I have been diagnosed with Ehlers Danlos syndrome, since my Sister died in 1996, and with it ankylosing spondylitis, among many, many other medical issues. In the beginning, we saw..

When to Suspect EDS- Ehlers Danlos Syndromes- Oh TWIS

Here is a detailed list of 47 different medication treatments for various pain syndromes: Amitriptyline for neuropathic pain and fibromyalgia in adults. Antidepressants for neuropathic pain. Antidepressants for pain management in rheumatoid arthritis. Antiepileptic drugs for neuropathic pain and fibromyalgia - an overview of Cochrane reviews Post category: Ankylosing Spondylitis / Ehlers-Danlos Syndrome / POTS For Emma, the worst part of receiving her diagnosis with ankylosing spondylitis wasn't adapting to the constant pain, losing her breath over five minutes of standing, being too exhausted t It may also occur in Ehlers-Danlos Syndrome, neurofibromatosis type I, ankylosing spondylitis, and is associated with spondylolisthesis, vertebral fractures, scoliosis, tumors or trauma. [13] In neurofibromatosis type I , it has been theorized that local infiltration of the dura by plexiform neurofibromas leads to a weakening of the dural.

Comorbidities Common with Ehlers Danlos Syndrom

Spoonies of all types are welcome to join us, but we will have a heavier focus on the lesser common, lesser understood, and difficult to diagnose conditions, such as Ehlers Danlos, Marfan's, Ankylosing spondylitis, Sjogren's syndrome, lupus, multiple sclerosis, sickle cell anemia, and endometriosis Ehlers-Danlos syndrome (EDS) is a group of inherited disorders that weaken connective tissues. Connective tissues are proteins that support skin, bones, blood vessels, and other organs. EDS usually affects your skin, joints and blood vessel walls. Symptoms include Loose joints Fragile, small blood vessels Abnormal scar formation and wound healing Soft, velvety, stretchy skin that [ Case Report: Ehlers-Danlos Syndrome Mimicking Vasculitis. A 43-year-old man with a past medical history of type 2 diabetes mellitus, bilateral inguinal hernia repair as a child and prior cholecystectomy woke from sleep with sudden-onset periumbilical abdominal pain. He was admitted to another hospital, but required transfer to our surgical. Ankylosing Spondylitis Awareness T-shirts and Gifts. Show support for Ankylosing Spondylitis with our blue awareness ribbon t-shirts and gifts. Wear the blue ribbon to help spread awareness for your loved one living with Ankylosing Spondylitis, or wear an inspirational design to keep yourself strong while fighting for a cure Dermatologic Signs of Systemic Disease Online Medical Reference - from diagnosis through treatment options. Co-authored by Lisa M. Grandinetti and Kenneth J. Tomecki of the Cleveland Clinic. The skin is often a window to systemic disease. By recognizing cutaneous manifestations of systemic diseases, the internist can often determine the appropriate diagnosis and therapy or the need for.

At the 18th Annual SPARTAN meeting for clinicians and researchers who care for patients with spondyloarthritis. Dr. Steven Vlad of Tufts University presented results of a study evaluating the awareness of primary care physicians of ankylosing spondylitis (AS) Ehlers-Danlos Syndrome Awareness T-shirts and Gifts. Show your support for Ehlers-Danlos Syndrome, with the black and white zebra ribbon awareness t-shirts and gifts. Support your loved one living with Ehlers-Danlos, or wear the zebra ribbon to keep yourself strong and spread awareness Ankylosing spondylitis, bursitis, carpal tunnel syndrome and degenerative disc disease are the types of arthritis treated at AFA in Bangalore. 91 9731611833 / 91 8277123567 Donate No

hypermobility Ehlers-Danlos syndrome (EDS) is the most common type. Etiology. caused by genetic alterations that affect collagen synthesis and processing. genetics. autosomal dominant or recessive. can also be acquired via a new spontaneous mutation. examples include. classic EDS Dural ectasia may also occur in Marfan's syndrome, Ehlers-Danlos syndrome and neurofibromatosis but in these conditions, unlike in ankylosing spondylitis, there is erosion into the posterior vertebral body. The mechanism of dural ectasia in ankylosing spondylitis is unclear. One hypothesis is that chronic inflammation reduces meningeal. Observational studies and case reports published since the early 1980s show that patients with spontaneous internal carotid artery dissection may also have a history of stroke in their family and/or hereditary connective tissue disorders, such as Marfan syndrome, Ehlers-Danlos syndrome, autosomal dominant polycystic kidney disease, pseudoxanthoma elasticum, fibromuscular dysplasia, and. Nov 11, 2020 - Explore Jeanmarie Skurka's board Ehlers Danlos Syndrome, followed by 424 people on Pinterest. See more ideas about ehlers danlos syndrome, ehlers danlos, syndrome

The Ehlers-Danlos syndromes (EDS) are currently classified into thirteen subtypes. Each EDS subtype has a set of clinical criteria that help guide diagnosis; a patient's physical signs and symptoms will be matched up to the major and minor criteria to identify the subtype that is the most complete fit The #backpain associated with #spondylitis can mean a constant battle against #pain. Do you ever feel like your pain has you juggling doctors, medicines, exercise, & healthy eating? Hop into the.. What others see is only part of the story. Find resources and support from other people living with #spondylitis An association between abnormal upper airway flaccidity and Ehlers- Danlos syndrome has been described in the absence of TBM (Ayres et al., 1981). We are unaware of any case of TBM occuring in association with ankylosing spondylitis

Ehlers-Danlos syndrome, type IV, or vascular Ehlers-Danlos syndrome, is an autosomal dominant disorder of connective tissue that mainly affects the arteries and digestive tract. The syndrome is caused by mutations of the COL341 gene, which codes for type III collagen The Ehlers-Danlos syndrome or SED refers to a group of inherited pathologies of the connective tissue that mainly affects the skin and joints, but can also affect other organs. SED affects connective tissues: tissues that support various parts of the body such as skin, muscles, tendons and ligaments. In the SED the collagen fibrous protein has.

Mast cell disorders in Ehlers-Danlos syndrome

Joint mobility and Ehlers-Danlos syndrome, (EDS) new data based on 232 cases. C. Hamonet, I Brock Hypermobility in Ehlers-Danlos syndrome was the first historical finding, and is still deemed by many to be a requirement for diagnosis To learn more about EDS, visit the website of the global community, The Ehlers-Danlos Society. Janna is a 36-year-old mother of two residing in Sydney's Eastern Suburbs with her young family. She lives with the chronic illness and rare disease, Ehlers-Danlos Syndrome

Ehlers-Danlos Syndrome(s) - Connecting the Dots! - Chiari

  1. Congenital collagenous compromise (e.g. syndromes: Down's, Ehlers-Danlos, Grisel, Morquio) Inflammatory arthritides (e.g. rheumatoid arthritis, ankylosing spondylitis) Recent neck/head/dental surgery. Characteristics/Clinical Presentation. There is a large agreement on following symptoms to make a clinical judgment on CCSI
  2. Spondylitis Association of America (SAA) is a national, non-profit organization, dedicated to being a leader in the quest to cure ankylosing spondylitis and related diseases, and to empower those affected to live life to the fullest. Ankylosing spondylitis information, ankylosing spondylitis treatment, ankylosing spondylitis forums, ankylosing spondylitis diagnosis, articles on ankylosing.
  3. Isabel M. from Chaps, New Mexico is living with Hypermobile Ehlers-Danlos syndrome, or hEDS. At the age of 22, she's already seen a lifetime of diagnoses. She's spent half of the past 2 years recovering from 5 surgeries and at the time of this posting, will be recovering from her 6th. And in her words, managing multiple conditions is like.
  4. ation In this episode, we discuss Shayla Symone's story with Ehlers Danlos Syndrome. She also has POTS, IBS, and Fibromyalgia. Shayla began to experience symptoms of EDS when she was in elementary school and was formally diagnosed in 2018/2019, a span of almost 15 years

Ehlers Danlos Syndromes Arthritis Foundatio

Ankylosing Spondylitis (AS) is a chronic inflammatory disease of unknown etiology characterized by prominent inflammation of spinal joints and adjacent structures. This inflammation leads to progressive fusion of the spine. Peripheral joints are less affected although the hips and shoulders may become involved in one third of cases What is Ehlers-danlos syndrome? Ehlers-danlos syndrome (group of inherited disorders that affect collagen structure and function) is found to be associated with 91 drugs and 35 conditions by eHealthMe.. What is Cellulitis? Cellulitis (infection under the skin) is found to be associated with 2,634 drugs and 2,003 conditions by eHealthMe Objectives To describe the epidemiology of diagnosed hypermobility spectrum disorder (HSD) and Ehlers-Danlos syndromes (EDS) using linked electronic medical records. To examine whether these conditions remain rare and primarily affect the musculoskeletal system. Design Nationwide linked electronic cohort and nested case-control study. Setting Routinely collected data from primary care and. Spine (Ankylosing spondylitis) Firmly held, fundamental belief about a specific subject that is based in untruth and illogic, and of course that means that everybody else's belief is wrong, wrong, wrong. Ehlers-Danlos syndrome Fear of abandonment that has manifested into the family's genetic makeup. Issues arising from the syndrome can be. Conditions within the Ehlers-Danlos spectrum are all connective tissue disorders. They are inherited and, as a group, quite rare. JHS and its cousin, hypermobile EDS, are exceptions to the rule. Both are fairly common compared to the other 11 disorders in the spectrum. Ehlers-Danlos conditions reduce the quality of collagen in the human body

Ehlers-Danlos syndrome: an update on classification by

  1. Welcome to The Spoonie Struggle! The show is about the raw, honest look at living life with chronic illnesses and chronic pain conditions. Spoonies of all types are welcome to join us, but we will have a heavier focus on the lesser common, lesser understood, and difficult to diagnose conditions, such as Ehlers Danlos, Marfan's, Ankylosing spondylitis, Sjogren's syndrome, lupus, multiple.
  2. Ehlers Danlos Syndrome Types Ehlers Danlos Hypermobility Elhers Danlos Syndrome Ankylosing Spondylitis Chronic Fatigue Symptoms Chronic Fatigue Syndrome Diet Chronic Pain Fibromyalgia Chronic Illness Thank goodness I don't have this symptom (yet), it's got to be horrible for those who d
  3. chronic illness, diagnosis, Ehlers-Danlos syndromes, Hypermobile Ehlers-Danlos syndromes, inherited condition, Life with Multiple Conditions Join Health Stories Project Health Stories Project was created to give people opportunities to share their personal health experiences and to learn from the experiences of others
  4. Learn more about Ankylosing Spondylitis and Spondyloarthropathies. Osteoarthritis. Osteoarthritis (OA) is the most common form of arthritis, affecting nearly 30 million adults nationwide. OA is an irreversible disease that causes deterioration of the joints. Doctors usually describe OA as wear and tear arthritis
  5. I tested positive for HLA B27 and have been diagnosed with Ehlers danlos can I have both ankylosing spondylitis and EDS. My mother had AS. 1 doctor answer • 1 doctor weighed in. Related topics. Ankylosing spondylitis. Spondylitis. Connect with a U.S. board-certified doctor by text or video anytime, anywhere

I am seeing a geneticist soon to confirm a diagnosis of Ehlers-Danlos syndrome (I have extremely hypermobile joints, especially hips). My hips/legs/butt/groin is in constant agony and the pain is my life. But yes, talk to a rheumatologist about Enbrel. It's an injection you administer yourself once a week (nowhere near as scary as it sounds Jul 29, 2020 - Explore Elizabeth Witte's board Ehlers Danlos - Hypermobility, followed by 161 people on Pinterest. See more ideas about ehlers danlos hypermobility, hypermobility, ehlers danlos

Jan 25, 2017 - Explore Kristi Kinchen's board ehlers danlos syndrome on Pinterest. See more ideas about ehlers danlos syndrome, ehlers danlos, syndrome Ankylosing spondylitis is associated with this but the diagnosis is made by physical exam and positive spine and hip x-rays. I have lots of patients with uveitis and hla b27 without other disease. I tested positive for HLA B27 and have been diagnosed with Ehlers danlos can I have both ankylosing spondylitis and EDS. My mother had AS Spondyloepiphyseal dysplasia congenita (abbreviated to SED more often than SDC) is a rare disorder of bone growth that results in dwarfism, characteristic skeletal abnormalities, and occasionally problems with vision and hearing.The name of the condition indicates that it affects the bones of the spine (spondylo-) and the ends of bones (), and that it is present from birth () Ehlers-Danlos syndromes (EDS) are a group of rare inherited conditions that affect connective tissue. Connective tissues provide support in skin, tendons, ligaments, blood vessels, internal organs and bones. Symptoms of Ehlers-Danlos syndromes (EDS) There are several types of EDS that may share some symptoms. These include

Ehlers-Danlos Syndrome and Sacroiliac Joint Dysfunctio

  1. ars, webinars, conferences, coaching and patient advocacy
  2. g fatigued, how to protect your joints from damage and what types of exercise best suit people with EDS. For more information on the importance of exercise and some ideas about different type
  3. 31 random facts about Ehlers-Danlos Syndrome (prounounced AY-lerz DAN-lowz), also known as EDS. It is a group of genetic disorders that are actually NOT rare - only rare to be properly diagnosed by a doctor who is knowledgeable about EDS
Cerebrovascular disorders: Cerebral Brain AneurysmSED / EDS / Syndrome d'Ehlers Danlos hypermobile - so they

DOI: 10.1016/0007-0971(81)90011-5 Corpus ID: 34625289. Haemoptysis and non-organic upper airways obstruction in a patient with previously undiagnosed Ehlers-Danlos syndrome. @article{Ayres1981HaemoptysisAN, title={Haemoptysis and non-organic upper airways obstruction in a patient with previously undiagnosed Ehlers-Danlos syndrome.}, author={J. Ayres and J. Rees and G. Cochrane}, journal. Costochondritis see Cartilage Disorders. Cramps see Muscle Cramps. Craniofacial Abnormalities. Craniosynostosis see Craniofacial Abnormalities. Cubital Tunnel Syndrome see Elbow Injuries and Disorders. Degenerative Joint Disease see Osteoarthritis. Dermatomyositis see Myositis. Diabetic Foot. Dislocated Shoulder

Ehlers Danlos Syndrome Types Ehlers Danlos Hypermobility Elhers Danlos Syndrome Sjogren's Syndrome Ankylosing Spondylitis Crps Chronic Fatigue Syndrome Invisible Illness Chronic Pain Chronic Fatigue Actual heart attacks are more likely with VEDS Syndrome Ehlers Danlos Ehlers Danlos Hypermobility Ankylosing Spondylitis Chronic Fatigue Syndrome Chronic Illness Chronic Pain Invisible Illness Autoimmune Disease Migraine EDS and Insomnia These adrenaline issues are also why we are more prone to anxiety and panic attacks Dr Mittal is a Consultant Rheumatologist and clinical lead for Ankylosing Spondylitis services at the Royal National Orthopaedic Hospital, Stanmore. She also holds appointments of Honorary Clinical Senior Lecturer, University College of London, and Honorary Visiting Scientist, Queen Mary University London Types of Arthritis. This guide explains the following types of Arthritis: Ankylosing Spondylitis, Calcium Pyrophosphate Dihydrate Crystal Deposition Disease, Ehlers-Danlos Syndrome, Fibromyalgia, Fifth Disease, Giant Cell Arteritis, Gout, Juvenile Arthritis, Lyme Disease, Myositis, Osteoarthritis, Psoriatic Arthritis, Raynaud's Phenomenon, Reactive Arthritis, Reflex Sympathetic Dystrophy.

Editor—The Ehlers-Danlos syndrome (EDS) is a diverse group of heritable connective tissue disorders whose primary clinical features include soft, hyperextensible skin, dystrophic scarring, easy bruising, and joint hypermobility.1 An initial classification defined 10 distinct types of EDS,1but with recent advances in our understanding of the molecular pathology a revised nosology with six. Dural ectasia describes widening of the dural sac or spinal nerve root sleeves, usually associated with bony erosions of the posterior vertebral body 4. One study suggests that the anteroposterior diameter of the thecal sac at the S1 level should be greater than that of the thecal sac at the L4 level in order to describe dural ectasia 4 Sept. 3, 2004 — Daily treatment with anakinra is effective in controlling the clinical manifestations of ankylosing spondylitis (AS), with a 61% improvement in spinal and sacroiliac joint (SIJ.

Crazy toes | Ehlers danlos syndrome, Ehlers danlos, Feet careInfographic: Profile of patients with PoTS (Most commonDegenerative disc disease | Rheumatoid Arthritis and