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To get horny for a long period of time.
Um, no. And if that lasts more than four hours, dude, call your doctor. ;-)
The Dermatosparaxis Type of EDS (formerly Type 7C) is extremely rare, with about 10 cases identified ever. It is characterized by extremely fragile, sagging skin and is caused by a defect in the ADAMTS2 gene. Mutations in this gene cause a dramatic reduction in the enzyme produced by this gene; the reduction in the enzyme means that procollagen is not processed correctly, so that collagen fibrils aren't formed correctly, so that the connective tissue within the body is very weak.
My understanding is that the common symptoms of the three more prevalent types (hypermobility, classic, and vascular) can be present in any of the more rare forms of EDS.
What else can I help you with?
What type of syndrome is the Koro syndrome?
Koro syndrome is a culture-bound syndrome characterized by an intense fear of retraction of the penis or shrinking of the genitals, leading to a belief that the genitals are disappearing or will disappear. It is primarily reported in certain Asian cultures. Treatment often involves reassurance, education, and addressing underlying cultural beliefs.
Which type of chromosomal abnormalities is most likely to be viable in humans?
Trisomy 21 (Down syndrome) is the most common type of chromosomal abnormality that is viable in humans. Individuals with Down syndrome have an extra copy of chromosome 21, which can result in distinctive physical characteristics and developmental delays, but many individuals with Down syndrome lead healthy and fulfilling lives.
What type of disorders are karyotyping used to diagnose?
Chromosomal disorders can be observed in a human karyotype. It can show whether there are extra chromosomes, or missing chromosomes, or malformed chromosomes, or whether chromosomes have extra pieces, or missing pieces.
What type of mutation causes marfan syndrome?
Marfan syndrome is typically caused by mutations in the FBN1 gene, which provides instructions for making a protein called fibrillin-1. These mutations can result in the production of an abnormal fibrillin-1 protein, leading to the characteristic features of Marfan syndrome such as tall stature, long limbs, and cardiovascular issues.
What type of mutation is marfan syndrome?
Marfan syndrome is a genetic disorder caused by mutations in the fibrillin-1 (FBN1) gene. These mutations can result in abnormalities in connective tissues, leading to symptoms such as tall stature, long limbs, heart defects, and eye problems.
How is Ehlers-Danlos Syndrome divided?
classical, hypermobility, vascular, kyphoscoliosis, arthrochalasia, and dermatosparaxis
What is Dermatosparaxis?
Skin fragility caused by abnormal collagen
How common is Ehlers-Danlos Syndrome?
Although it is difficult to estimate the overall frequency of Ehlers-Danlos syndrome, the combined prevalence of all types of this condition may be about 1 in 5,000 individuals worldwide. The hypermobility and classic forms are most common; the hypermobility type may affect as many as 1 in 10,000 to 15,000 people, while the classic type probably occurs in 1 in 20,000 to 40,000 people. Other forms of Ehlers-Danlos syndrome are very rare. About 30 cases of the arthrochalasia type and fewer than 60 cases of the kyphoscoliosis type have been reported worldwide. About a dozen infants and children with the dermatosparaxis type have been described. The vascular type is also rare; estimates vary widely, but the condition may affect about 1 in 250,000 people.
Can you write a sentence using the word syndrome?
no one in my family has no type of syndrome
What is the type of mutation that causes Digeorge syndrome?
Deletion Mutation causes DiGeorges Syndrome.
Can a baby get shaken baby syndrome from earthquake?
No. The type of shaking in an earthquake is not the same as the type needed to cause shaken baby syndrome.
Can Down syndrome be considered a type of cancer?
No
Is POEMS syndrome a type of cancer?
yes
What is central pain syndrome?
Central pain syndrome is a type of pain that occurs because of injuries to the brain or spinal cord.
What chromosome is affected by meckel syndrome?
Meckel Syndrome (type 1)is an autosomal recessive trait carried on chromosome 17.
The lazy eye syndrome is a type of strabismus called?
amblyopia
What type of doctor treats piriformis syndrome?
orthopedic surgeon
