At what age is Ehlers-Danlos syndrome diagnosed?

It is usually diagnosed before the age of 2 years. Fragility, bruising and sagging of the skin are severe but, surprisingly, the skin heals well. Like the other rare types, in order to inherit it you need to inherit one faulty gene from EACH of your parents.

How do I know if my child has Ehlers-Danlos syndrome?

Hypermobile EDS: Typical symptoms include joint hypermobility; soft, velvety skin that bruises easily; and chronic bone or muscle pain. Classical EDS: Symptoms may include elastic, stretchy skin that bruises easily, hypermobile joints, muscle weakness, and delayed development.

When can EDS be diagnosed?

My geneticist told me that it often takes an average of 10 to 20 years to receive a diagnosis of EDS, with many people not receiving an accurate diagnosis until well into their 40s. As with many medical conditions, EDS disproportionately impacts women.

What triggers EDS?

Causes. EDS happens when your body doesn't make a protein called collagen in the right way. Collagen helps form the connections that hold your body's bones, skin, and organs together. If there's a problem with it, those structures can be weak and more likely to have problems.

How do you know if you have EDS?

Extremely loose joints, fragile or stretchy skin, and a family history of Ehlers-Danlos syndrome are often enough to make a diagnosis. Genetic tests on a sample of your blood can confirm the diagnosis in rarer forms of Ehlers-Danlos syndrome and help rule out other problems.

The Ehlers-Danlos Syndromes (EDS)

What mimics Ehlers-Danlos syndrome?

Tnxb-/- mice showed progressive skin hyperextensibility, similar to individuals with Ehlers-Danlos syndrome. Biomechanical testing confirmed increased deformability and reduced tensile strength of their skin.

Can you have EDS and not know it?

Milder forms of EDS are often not diagnosed until early adulthood, as it can take some time before the symptoms and signs become noticeable. The more severe types, however, are diagnosed mainly in childhood. Some types have been seen so few times that it is hard to generalise about what symptoms are normal for them.

What kind of doctor manages Ehlers-Danlos?

Successful treatment of this complex syndrome requires a team with extensive knowledge of genetics, orthopedics, pediatrics, neurology, neuroradiology, neuropsychology, and neuroendocrinology, in addition to skilled surgeons who specialize in neurosurgery and cerebrovascular surgery.

Is EDS a sleep disorder?

Abstract. The Ehlers-Danlos syndrome (EDS) is an inherited heterogeneous group of connective tissue disorders, affecting tissue fragility, blood vessels, and other organs. EDS patients are known to suffer from significant sleep problems and excessive daytime sleepiness.

What are the 14 types of Ehlers-Danlos?

Does Ehlers-Danlos get worse with age?

Many of the problems associated with EDS are progressive, meaning that they get worse over time. Kyphoscoliosis EDS (kyphosis and scoliosis) is a form of Ehlers-Danlos Syndrome that is noted for severe, progressive curvature of the spine.

Are you born with EDS?

EDS is something you are born with but symptoms may not manifest themselves until later in life. It is not uncommon for a genetic condition to first become apparent during puberty, alternatively symptoms can be triggered by a trauma, such as a virus, many years down the line.

Does 23 and ME test for EDS?

This article will discuss some conditions that are not included in 23andMe reports. If you are interested in learning about which conditions are included in the 23andMe Health + Ancestry Service, you can view a full list here. 23andMe does not offer diagnostic testing.

Is EDS linked to autism?

Recent research suggests that EDS may share strong links with autism. Case studies have previously been published identifying individuals who are both on the autism spectrum and have a diagnosis of EDS.

Can you develop EDS?

Different types of Ehlers-Danlos syndrome are associated with a variety of genetic causes, some of which are inherited and passed on from parent to child. If you have the most common form, hypermobile Ehlers-Danlos syndrome, there's a 50% chance that you'll pass on the gene to each of your children.

Can you have Ehlers-Danlos without hypermobility?

Indeed, each type of Ehlers-Danlos is a distinct disorder with its own unique symptoms and challenges—and many do not present with joint hypermobility as a defining symptom. And, unlike hEDS, every other form of EDS results from an identified genetic variant.

Do people with EDS sleep more?

Abstract. Background Patients with the connective tissue disorder Ehlers-Danlos syndrome (EDS) often suffer from fatigue, excessive daytime sleepiness and impaired quality of life. Obstructive sleep apnoea (OSA) may be an underlying cause for these symptoms but its prevalence in this population is unclear.

Can EDS affect breathing?

Persons with the Ehlers-Danlos syndromes (EDS) report a wide range of respiratory symptoms, most commonly shortness of breath, exercise limitation, and cough. Also reported are noisy breathing attributed to asthma, difficulty with deep inhalation, and inspiratory thoracic pain.

Why does EDS cause insomnia?

Some studies have indicated that the autonomic nervous system is not functioning properly in patients with hypermobile EDS. Moreover, many patients experience chronic pain and fatigue, which may cause sleep disturbances or make it more difficult to get enough restful sleep.

Where can I get an EDS diagnosis?

Your GP may refer you to a joint specialist (rheumatologist) if you have problems with your joints and they suspect EDS. If there's a possibility you may have 1 of the rare types of EDS, your GP can refer you to your local genetics service for an assessment.

Can a dermatologist diagnose Ehlers-Danlos?

Diagnosis of these rare conditions is challenging and recognition of EDS by the dermatologist can facilitate accurate diagnosis by genetic testing. This enables genetic counselling and targeted management to optimize both quality of life and life expectancy in these patients.

Where can I get diagnosed with Ehlers-Danlos syndrome?

Most medical doctors should be able to diagnose EDS and HSD. However, because the Ehlers-Danlos syndromes are genetic disorders, primary care physicians often provide their patients with referrals to a geneticist.

Does Ehlers-Danlos make you look younger?

Due to the collagen in the skin being extra stretchy, many EDS patients experience a lack of wrinkles as they age. This collagen may help EDS patients look younger and can also cause skin to feel extremely soft. Doctor's even describe the skin as “velvet-soft”.

What does an EDS flare up feel like?

Day 4 of the Photo-A-Day Challenge - What does a flare up (of symptoms) look like for you? "A "flare up" with EDS for me is extreme pain with my joints, a low grade fever, and subluxations of my fingers and other joints. "Today you are actually witnessing one of the longest flares I've had since being diagnosed.

How does Ehlers-Danlos affect hair?

The defects of the collagen previously reported in EDS account for the increased extensibility of the skin (1, 2). It is possible that the altered skin structure results in increased pliability of the skin which may allow the hair follicles to expand.