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Definition. A skin texture that is unusually soft (and may feel silky), and has a malleable consistency resembling that of dough. [
Why is my skin so doughy?
Dermatosparaxis Ehlers-Danlos syndrome (dEDS) is an inherited connective tissue disorder that is caused by defects in a protein called collagen. Common symptoms include soft, doughy skin that is extremely fragile; saggy, redundant skin, especially on the face; hernias; and mild to severe joint hypermobility.
How many people have Dermatosparaxis EDS?
Dermatosparaxis EDS is an example of an extremely rare type of EDS, with only a few cases recorded in medical literature. Vascular EDS is reported to have a prevalence of 1 in 100,000 individuals, and cardiac-valvular EDS a prevalence of less than 1 in a million people.
What is the life expectancy of someone with hypermobile Ehlers-Danlos syndrome?
Patients with the classical and hypermobility forms of Ehlers-Danlos syndrome have a normal life expectancy. About 80% of patients with vascular Ehlers-Danlos syndrome will experience a major health event by age 40 and the life expectancy is shortened, with an average age of death of 48 years.
How rare is classical like EDS?
When both parents carry one copy of the mutated TNXB gene, their child has a 25% chance of inheriting classical-like EDS. There is a 50% chance of the child inheriting one mutated copy from either parent in which case they become a carrier.
Nigel Burrows – Skin Changes in EDS
45 related questions found
Can you have EDS without stretchy skin?
Skin and Connective Tissue: People with hEDS do NOT have to have profoundly stretchy skin! Most notably, in hEDS, the degree of softness, stretchiness, fragility, bruisability, and poor wound healing of skin differs from “normal” subjects but is mild in comparison to other types of EDS.
What is Ehlers-Danlos type 4?
Ehlers-Danlos syndrome type IV, the vascular type of Ehlers-Danlos syndromes (EDS), is an inherited connective tissue disorder defined by characteristic facial features (acrogeria) in most patients, translucent skin with highly visible subcutaneous vessels on the trunk and lower back, easy bruising, and severe arterial …
Does EDS make you skinny?
Ehlers-Danlos syndrome (EDS) is a disease that weakens the connective tissues of your body. These are things like tendons and ligaments that hold parts of your body together. EDS can make your joints loose and your skin thin and easily bruised.
Can you live a long life with vEDS?
Currently, the median life span is about 51 years-within a wide range from 10 to 80 years-and it is influenced by the nature of the particular COL3A1 variant. A vEDS diagnosis is most often sought because of family history; someone’s medical history; or pregnancy complications at a young age.
At what age is Ehlers-Danlos Syndrome diagnosed?
The age at first diagnosis peaked in the age group 5-9 years for men and 15-19 years for women (see figure 2). There was a significant difference of 8.5 years in the mean age of diagnosis between men and women (95% CI: 7.70 to 9.22): 9.6 years in EDS (95% CI: 6.85 to 12.31) and 8.3 years in JHS (95% CI: 7.58 to 9.11).
What does EDS pain feel like?
Pain in the abdomen. Frequent headaches. Pain with daily tasks. People with EDS can have trouble using pens and pencils, because holding tightly to something so thin becomes painful.
Is Ehlers Danlos a disability?
Can I Get Disability For Ehlers-Danlos Syndrome (EDS)? The answer is that Ehlers-Danlos Syndrome (EDS) can be a disabling condition, depending on how it presents. EDS is a genetic disorder affecting connective tissues and causing an array of serious physical problems, ranging from joint pain to cardiovascular issues.
Can EDS skip a generation?
In some dominant conditions, it is possible for someone to inherit an altered gene without showing any or all symptoms of the condition. This person could then go on to have an affected child, which may make the disease appear to have skipped a generation.
How can I regain elasticity in my skin?
- Collagen supplements. Collagen is a protein found in the skin’s connective tissues. …
- Retinol and retinoids. Retinol is a form of vitamin A. …
- Hyaluronic acid. …
- Genistein isoflavones. …
- Hormone replacement therapy (HRT) …
- Witch hazel extract. …
- Cocoa flavanols. …
- Laser treatments.
What medical conditions cause saggy skin?
Another condition that causes saggy skin is Ehlers-Danlos syndrome (EDS), a rare, connective tissue disorder that is inherited. People with EDS have a defect in collagen production that results in saggy, doughy skin, often on the face.
What does it mean when your skin is translucent?
Translucent skin is defined as an increased ability of the skin to pass light through it and allow typically hidden features such as veins or tendons to be more visible through the skin.
What does VEDS feel like?
Emergency care is needed immediately. Symptoms include: Sudden onset pain; may be “severe,” “sharp,” “tearing,” or “ripping” and may be located anywhere in the body, depending on which artery is affected. Sometimes, the pain is less severe, but a person still has a feeling that “something is very wrong.”
Can you have mild VEDS?
Children with vascular Ehlers-Danlos syndrome can have mild or severe signs and may have characteristic facial features such as a small chin, thin nose and lips, and deep-set, large eyes.
Are you born with VEDS?
People with VEDS are born with it, but features of the condition are not always present right away. Some people have signs of VEDS at birth or as young children – including conditions like congenital clubfoot, hip dislocation, limb deformity and visible veins.
Does EDS affect hair?
Ehlers-Danlos syndromes primarily affects the skin, hair, and skeletal system. Symptoms usually begin by childhood or adolescence. Like people with other types of EDS, people with Spondylodysplastic EDS have unusually flexible joints; loose, elastic skin; and easy scarring.
Does EDS affect the eyes?
Ehlers Danlos Syndrome patients are prone to myopia and elongated eyes due to the stretching of the collagenous sclera.
What percentage of people with EDS are underweight?
People in Larger Bodies Eating Disorder Statistics
Less than 6% of people with eating disorders are medically diagnosed as “underweight.”
What is Arthrochalasia?
Arthrochalasia Ehlers-Danlos syndrome (aEDS) is an inherited connective tissue disorder that is caused by defects in a protein called collagen. Common symptoms include severe joint hypermobility; congenital hip dislocation; fragile, hyperextensible skin; hypotonia ; and kyphoscoliosis (kyphosis and scoliosis ).
How is hed diagnosed?
There is no test for hEDS, so diagnosis involves looking for joint hypermobility, signs of faulty connective tissue throughout the body (e.g. skin features, hernias, prolapses), a family history of the condition, and musculoskeletal problems (e.g. long-term pain, dislocations).
How common is EDS type 4?
The estimated prevalence for all EDS varies between 1/10,000 and 1/25,000, EDS type IV representing approximately 5 to 10% of cases. The vascular complications may affect all anatomical areas, with a tendency toward arteries of large and medium diameter.