Simmonds’ disease or pituitary cachexia is a syndrome ascribed to destruction or physiological exhaustion of the hypophysis (chiefly the anterior portion). The destruction may be caused by embolic infarction, tumor, syphilis, tuberculosis, metastatic abscesses, inflammation, etc.

What is the giant disease called? Acromegaly is a hormonal disorder that develops when your pituitary gland produces too much growth hormone during adulthood. When you have too much growth hormone, your bones increase in size. In childhood, this leads to increased height and is called gigantism.

also,  What is Hypopituitary? Hypopituitarism is a rare disorder in which your pituitary gland fails to produce one or more hormones, or doesn’t produce enough hormones. The pituitary gland is a kidney-bean-sized gland situated at the base of your brain.

What is Sheehan’s syndrome? Sheehan’s syndrome is a condition that affects women who lose a life-threatening amount of blood in childbirth or who have severe low blood pressure during or after childbirth, which can deprive the body of oxygen. This lack of oxygen that causes damage to the pituitary gland is known as Sheehan’s syndrome.

What is Wilson syndrome?

Wilson’s disease is a rare inherited disorder that causes copper to accumulate in your liver, brain and other vital organs. Most people with Wilson’s disease are diagnosed between the ages of 5 and 35, but it can affect younger and older people, as well.

similary What famous person has acromegaly?

5. The high mortality of untreated acromegaly is illustrated by the short lives of wrestler Andre “The Giant” Rousimoff and actor Rondo Hatton.

What is a Craniopharyngioma? Enlarge. Craniopharyngiomas are rare brain tumors that usually form near the pituitary gland and the hypothalamus. They are benign (not cancer) and do not spread to other parts of the brain or to other parts of the body.

What is Sotos? Sotos syndrome is a disorder characterized by a distinctive facial appearance, overgrowth in childhood, and learning disabilities or delayed development of mental and movement abilities. Characteristic facial features include a long, narrow face; a high forehead; flushed (reddened) cheeks; and a small, pointed chin.

What is the pituitary?

The pituitary gland is a small, bean-shaped gland situated at the base of your brain, somewhat behind your nose and between your ears. Despite its small size, the gland influences nearly every part of your body. The hormones it produces help regulate important functions, such as growth, blood pressure and reproduction.

What is empty sella? Empty sella syndrome (ESS) may occur if you have an enlarged sella turcica. This is a bony structure where the pituitary gland sits at the base of the brain. During an imaging test of the area, the pituitary gland may first look like it is missing.

What is a galactorrhea?

Overview. Galactorrhea (guh-lack-toe-REE-uh) is a milky nipple discharge unrelated to the normal milk production of breast-feeding. Galactorrhea itself isn’t a disease, but it could be a sign of an underlying problem. It usually occurs in women, even those who have never had children or after menopause.

What is empty sella syndrome? Empty sella syndrome (ESS) may occur if you have an enlarged sella turcica. This is a bony structure where the pituitary gland sits at the base of the brain. During an imaging test of the area, the pituitary gland may first look like it is missing.

Is panhypopituitarism a rare disease?

What is Panhypopituitarism? What is the prevalence of Panhypopituitarism? Internationally, hypopituitarism has an estimated incidence of 4.2 cases per 100,000 per year and an estimated prevalence of 45.5 cases per 100,000 without gender difference.

What is Carpenter’s syndrome?

Carpenter syndrome is a condition characterized by the premature fusion of certain skull bones (craniosynostosis), abnormalities of the fingers and toes, and other developmental problems. Craniosynostosis prevents the skull from growing normally, frequently giving the head a pointed appearance (acrocephaly).

What is Noonan syndrome? Noonan syndrome is a condition that some babies are born with. It causes changes in the face and chest, usually includes heart problems, and slightly raises a child’s risk of blood cancer (leukemia). Noonan syndrome is a pretty common condition, affecting 1 in 1,000–2,500 babies.

What is Kleefstra syndrome? Kleefstra syndrome is a disorder that involves many parts of the body. Characteristic features of Kleefstra syndrome include developmental delay and intellectual disability, severely limited or absent speech, and weak muscle tone (hypotonia).

What is the life expectancy of someone with acromegaly?

in 1970, nearly 20 studies have analyzed mortality rates in over 5,000 patients with acromegaly. Overall standardized mortality rates are approximately two times higher than in the general population, relating to an average reduction in life expectancy of around 10 years.

How old do people live with gigantism? When the condition is successfully treated, children with gigantism can have a normal life expectancy and avoid most of the complications caused by it. However, they may still have symptoms such as muscle weakness and restricted movement, and some may also have psychological problems.

Did jaws have gigantism?

Early life. Kiel was born in Detroit, Michigan. His extraordinary height was a result of acromegaly, a condition caused by an excess of human growth hormone.

What is a chordoma? Chordoma is a slow growing cancer of tissue found inside the spine. Chordoma can happen anywhere along the spine. It is most often found near the tailbone (called a sacral tumor) or where the spine meets the skull (called a clival tumor). Chordoma is also called notochordal sarcoma.

What is Macroadenoma?

A macroadenoma is a tumor that typically develops in the pituitary gland, a pea-sized organ behind the eyes. They are almost always noncancerous.

What is Canavan’s? Collapse Section. Canavan disease is a rare inherited disorder that damages the ability of nerve cells (neurons) in the brain to send and receive messages. This disease is one of a group of genetic disorders called leukodystrophies.

What is Trisomy 14 called?

General Discussion. Chromosome 14, Trisomy Mosaic is a rare chromosomal disorder in which chromosome 14 appears three times (trisomy) rather than twice in some cells of the body. The term “mosaic” indicates that some cells contain the extra chromosome 14, whereas others have the normal chromosomal pair.

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