The following Conditions are related to Constipation

Select a specific condition below to view its details.

  • E-d syndrome

    E-d syndrome is known as Ehlers- Danlos syndrome, EDS, or elastic skin. This is a type of disorder that mainly affects connective tissue. It is basically a genetic disorder.E-d syndrome is a dominant or recessive genetic condition.E-d syndrome occurs when only a single copy of an abnormal gene is inherited from either parent or can be the result of a new mutation (gene change) in the affected individual.  Read More

  • Ehlers danlos syndrome

    Ehlers- Danlos syndrome, EDS, or elastic skin, is a type of disorder that mainly affects connective tissue. It is basically a genetic disorder.E-d syndrome is a dominant or recessive genetic condition.E-d syndrome occurs when only a single copy of an abnormal gene is inherited from either parent or can be the result of a new mutation (gene change) in the affected individual.There are 50% chance of  Read More

  • Riley-day syndrome

    A hereditary genetic abnormality known as Riley-Day syndrome affects the neurological system of the human body.Dysautonomia, or injury to the autonomic nervous system, results in abnormalities in the autonomic nervous system, which links the brain and spinal cord to the muscles and produces autonomic dysfunction.The body might lose the ability to detect touch, smell, and pain as a result of certain disorde  Read More

  • Systemic sclerosis

    The symptoms and severity of the disorder vary from one person to another based on the systems and organs involved. Skin It is very common to experience hardening and tightening of patches of your skin with SS. The patches may be oval-shaped or a straight line that can cover large areas of your skin. Your skin may also appear shiny since it’s so tight with your movement restricted. F  Read More

  • Ws -- waardenburg syndrome

    Waardenburg syndrome (WS) is a group of genetic disorders named after Dutch ophthalmologist and geneticist Petrus Johannes Waardenburg, who described it. This is an autosomal dominant inherited disorder. This rare disease results in the loss of pigmentary cells in the eyes, skin, stria vascularis of the cochlea, and hair.This type of disease may cause features like facial abnormalities like the diminished coloratio  Read More