Postural orthostatic tachycardia syndrome (POTS) is one of a group of disorders that have orthostatic intolerance (OI) as their primary symptom. OI describes a condition in which an excessively reduced volume of blood returns to the heart after an individual stands up from a lying down position. Who gets POT syndrome? Capgras syndrome is most commonly associated with Alzheimer’s disease or dementia. Both of these affect memory and can alter your sense of reality. Schizophrenia, especially paranoid hallucinatory. WILSON SYNDROME: Congenital defect in Ceruloplasmin, leading to buildup of copper - mental retardation, cirrhosis, hepatolenticular degeneration. ENDOCRINE, REPRODUCTIVE AMENNORRHEA-GALACTORRHEA SYNDROME: Non-physiologic lactation, resulting from endocrinologic causes or from a pituitary disorder.

What is Asherman’s syndrome?

Asherman’s syndrome is an acquired condition (one you are not born with) that refers to having scar tissue in the uterus or in the cervix (the opening to the uterus). This scar tissue makes the walls of these organs stick together and reduces the size of the uterus. Asherman’s syndrome is also known as intrauterine synechiae or uterine synechiae. Synechiae means adhesions. Asherman’s syndrome is also called intrauterine adhesions (IUA).

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How common is Asherman’s syndrome?

Asherman’s syndrome is considered a rare disease. It is hard to say how often it actually occurs because it is not always diagnosed. Some research estimates that IUA happen in nearly 20% of women who have had dilation and curettage (D&C) after pregnancy complications.

What are the symptoms of Asherman’s syndrome?

Having very light periods (hypomenorrhea)
Having no periods (amenorrhea)
Having severe cramping or pain
Being unable to get or stay pregnant

Some women have no symptoms, and some women have normal periods.

What causes Asherman’s syndrome?

Scar tissue from uterine surgery like dilation and curettage (D&C). (This is the cause of more than 90% of IUA.)
Scar tissue after a Cesarean section or from sutures used to stop hemorrhages
Endometriosis
Infections of the reproductive organs
Radiation treatment

What is DiGeorge syndrome?

DiGeorge syndrome is a genetic disorder that can affect many parts of the body. These problems, usually present at a baby’s birth or in early childhood, include heart defects, an impaired immune system and developmental delays.

Most people with DiGeorge syndrome are missing a small piece of chromosome 22 known as 22q11.2. (The condition is also known as 22q11.2 deletion syndrome.)

DiGeorge syndrome is a primary immunodeficiency disease (PIDD). These genetic disorders cause problems with the immune system.

Problems stemming from DiGeorge syndrome can range from mild to life-threatening.

How common is DiGeorge syndrome?

DiGeorge syndrome isn’t common. Only about 1 out of 4,000 people in the U.S. is diagnosed with the disorder every year.

Syndrome X

What are the symptoms of DiGeorge syndrome?

Angelman Syndrome

Symptoms of DiGeorge syndrome can range from minor to severe and vary from person to person.

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In some cases people with DiGeorge syndrome have no symptoms at all. Sometimes they have distinctive facial features including hooded eyelids, cheek flatness, a prominent bulbous nasal tip, an underdeveloped chin, or ears that appear prominent with attached lobes. These features will vary from person to person.

Symptoms of DiGeorge syndrome may include:

Syndrome Meaning

Breathing difficulties.
Developmental disabilities including learning and behavioral problems.
Heart defects (congenital heart disease).
Hypocalcemia (lower than normal levels of calcium in the blood), which can cause a seizure disorder.
Immune system problems including increased infections and pneumonias due to impaired production of T-lymphocyte (white blood cells that fight infection).
Kidney abnormalities.
Endocrine (hormonal) system problems.
Speech issues including hypernasal speech.
Cleft lip and palate (opening in the lip or roof of the mouth).

What causes DiGeorge syndrome?

Tissue that forms abnormally during a baby’s development causes DiGeorge syndrome. In most cases, this congenital (present at birth) disability occurs when a small piece of chromosome 22 is missing.

Syndrome Vs Disease

The affected part of chromosome 22 includes dozens of genes related to the development of several systems in the body. When part of this chromosome is missing, related organs and systems don’t develop normally.

Syndrome

Easy pose download free. In a small number of cases, DiGeorge syndrome is hereditary (passed from a parent to a child). Most of the time the gene mutation (change) that causes DiGeorge syndrome happens randomly.