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Doctor insights on: Cushing Syndrome

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What is Cushing syndrome?

What is Cushing syndrome?

Cushing syndrome: read this: http://en.wikipedia.org/wiki/Cushing%27s_syndrome

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Dr. Liuska Pesce
288 doctors shared insights

Cushing's Syndrome (Definition)

A medical condition caused by excess amount of cortisol in the body. Cushing's syndrome is usually the result of taking too much corticosteroid medications vs. a condition called Cushing's disease, where the body makes too much cortisol. ...Read more


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What is antiphospolipid syndrome (hughes syndrome)?

What is antiphospolipid syndrome (hughes syndrome)?

Antiphospholipids: An autoimune disorder characterized by antibodies to certain phopholipids that predisposes to clotting problmes and pregnancy complications. A certain percentage will develop into systemic lupus. ...Read more

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What is cushing's syndrome?

What is cushing's syndrome?

Symptom / sign mix: The familiar physical changes from excess glucocorticoids from any cause, made in the body or prescribged. Red, swollen face, hypertension, glucose intolerance, truncal obesity, fat pad on back of neck, fragile skin, likelihood to get infections, mood problems, acne, more. Contrast "cushing's disease" in which these by definition result from a pituitary adenoma making acth. ...Read more

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Adrenal fatigue syndrome, treatment?

Adrenal fatigue syndrome, treatment?

Many possibilities.: There are innumerable medical, nutritional and emotional conditions that include being tired as a symptom. These range from simple issues to those far more complex. A good checkup and blood testing would be a good starting point. If you're embarking on a regimen for adrenal fatigue, just make sure the diagnosis is accurate and the work up is complete. ...Read more

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What's turner syndrome?

What's turner syndrome?

45 X/0 Pattern: At conception, one half of a set of 46 (23pairs) chromosomes (cms) is brought from egg & sperm.If the combination is missing one x of the sex cms, a female is born with 45 instead of 46 cms, to reflect the loss.The lost cms can effect every cell in the body, resulting in a variety of heart, kidney, brain or other problems. It also may cause no specific problem & not be noticed until lat childhood. ...Read more

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What are frey syndrome, horner's syndrome and shy-drager syndrome?

What are frey syndrome, horner's syndrome and shy-drager syndrome?

What do they have in: They all have abnormalities of autonomics and other nervous sytem problems. ...Read more

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Is paraneoplastic syndrome genetic?

Is paraneoplastic syndrome genetic?

No: There is no genetic relationship to the development of a paraneoplastic syndrome. ...Read more

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Is prader willi syndrome hereditary?

Is prader willi syndrome hereditary?

Not typically: Prader willi is most commonly a random genetic abnormality that occurs early in development of fetus. There is usually no history of the disease in the family. ...Read more

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What's evans syndrome?

What's evans syndrome?

Anemia: Evans syndrome is a rare type of anemia in which the body makes antibodies that destroys white blood cells, red blood cells and platelets. ...Read more

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What's hughes syndrome?

What's hughes syndrome?

Autoimmune clotting: Try here: http://www.Hughes-syndrome.Org/symptoms.Htm.

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What is prader willi syndrome?

A genetic disorder: Usually from a deletion of a gene on the chromosome 15 inherited from the father, it can also come from having both chr 15's from the mother or both acting as if they came from mother. Infants have low muscle tone & trouble gaining weight; food craving & weight gain start about 18 mos. They have congenital anomalies, intellectual disability, compulsive behavior, & medical problems due to obesity. ...Read more

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Which person discovered crouzonodermoskeletal syndrome (crouzon syndrome)?

Which person discovered crouzonodermoskeletal syndrome (crouzon syndrome)?

Crouzon: Crouzon craniofacial dysostosis was described by crouzon in 1912. The genetic cause was not identified until 1994 and the credit goes to a number of different geneticists - reardon and preston independently helped narrow the genetic inheritance to the fgfr2 gene. ...Read more

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Goldenhar syndrome treatment?

Goldenhar syndrome treatment?

Birth defect: Congenital birth defect that affects the development of the ear, nose, mandible, and palate. ...Read more

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Whats compartment syndrome?

Whats compartment syndrome?

CS: It is a very severe and serious condition that can result in nerve and muscle damage if not treated. It results from pressure on those tissues, often from fracture, crush injury or lack of blood flow to the tissue. ...Read more

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Why there's hirsutism in cushing's syndrome?

Why there's hirsutism in cushing's syndrome?

Adrenal androgens: When the adrenals are stimulated, they make cortisol, but also androgens, like DHEA-S, which causes hirsutism in women. ...Read more

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Symptoms of polycystic ovarian syndrome?

Symptoms of polycystic ovarian syndrome?

Irregular cycles ...: Most women with pcos have one or more of: irregular periods or no cycles, acne, oily skin, unwanted hair growth especially on the face or lower stomach, infertility or subfertility (difficulty getting pregnant). Some women with pcos have little or no symptoms - we look at symptoms, blood tests and an ultrasound of the ovaries to make the diagnosis. Not all women with pcos have fertility issues. ...Read more

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Is nephrotic syndrome hereditary?

Is nephrotic syndrome hereditary?

See below: Some causes of nephrotic syndrome are due to herediary causes, eg one of the causes of fsgs also called focal and segmentalglomerulosclerosis. ...Read more

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Is munchausen syndrome herreitery?

Possibly: There may be some hereditary predisposition. Munchausen syndrome was reported in two brothers, two twins and couple families. ...Read more

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What causes turner syndrome?

Lack of chromosome: Normal humans have 22 pairs of regular chromosomes (chms) and one pair of sex chms .At conception you are supposed to get one of each pair from each parent. If one of the sex (X) chms is lost from the egg, the fetus (which can survive the mistake) will be born with 22 pr of regular chms and only one X.The defect occurs in the formation of the egg. The effect on the kid varies. ...Read more

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