Glossary for Heat intolerance

Medical terms related to Heat intolerance or mentioned in this section include:

• Andrade's syndrome: An inherited condition characterized by deposits of an abnormal protein called amyloid in various parts of the body including organs. The condition mainly involves neurological symptoms.
• Anterior pituitary hyperhormonotrophic syndrome: A syndrome characterized by the excessive production of various hormones (gonadotrophic, thyrotrophic, lactotrophic and pancreatrophic hormone).
• Athabaskan severe combined immunodeficiency: A severe immunodeficiency disorder found in Navajo and Apache populations.
• Bradbury-Eggleston syndrome: A syndrome mainly involving reduced blood pressure, lightheadedness or fainting on standing, dizziness and visual disturbances that is associated with a degeneration of the autonomic nerve system. It is most common in older males. Symptoms tend to be worse in the morning, after eating, after exercise or in hot weather.
• Chills: Excessive feeling of coldness.
• Common symptoms: The most common symptoms
• Ectodermal dysplasia anhidrotic: A rare inherited condition involving skin, hair, teeth and nail abnormalities. The condition is characterized by the absence of sweat and sebaceous glands, underdeveloped hair and teeth, characteristic face and other physical deformities.
• Ectodermal dysplasia, anhidrotic with T-cell immunodeficiency, autosomal dominant: An inherited disorder characterized by dry, rough skin, sparse scalp hair, cone-shaped teeth and an immune system disorder.
• Fever: Raised body temperature usually with other symptoms.
• Graves Disease: A condition which is an autoimmune disease that affects the thyroid resulting hyperthyroidism
• Hay-Wells Syndrome: A rare genetic disorder characterized by ankyloblepharon, ectodermal dysplasia, and cleft lip and/or cleft palate.
• Hay-Wells syndrome, recessive type: A rare recessively inherited genetic disorder characterized by ankyloblepharon, ectodermal dysplasia, and cleft lip and/or cleft palate. The recessive form of this condition is distinguished by the presence at birth of adhesions between the upper and lower jaws.
• Hyperthyroidism: The excessive activity of the thyroid gland
• Hypothyroidism: The decreased activity of the thyroid gland
• Lamellar ichthyosis: A very rare disorder where an infant is born covered with a transparent membrane which sheds to reveal red scaly skin patches of varying sizes.
• Lamellar ichthyosis, autosomal dominant form: A very rare dominantly inherited disorder where an infant is born covered with a transparent membrane which sheds to reveal red scaly skin patches of varying sizes.
• Lamellar ichthyosis, type 1: A very rare disorder where an infant is born covered with a transparent membrane which sheds to reveal red scaly skin patches of varying sizes. Type 1 is distinguished by the location of the genetic defect - chromosome 14q11.2.
• Lamellar ichthyosis, type 2: A very rare disorder where an infant is born covered with a transparent membrane which sheds to reveal red scaly skin patches of varying sizes. Type 2 is distinguished by the location of the genetic defect - chromosome 2q34.
• Lamellar ichthyosis, type 3: A very rare disorder where an infant is born covered with a transparent membrane which sheds to reveal large dark, plate-like scales. Type 3 is distinguished by the location of the genetic defect - chromosome 19p12-q12. This type also affects the ears and face to a greater degree than other types.
• Lamellar ichthyosis, type 5: A very rare disorder where an infant is born covered with a transparent membrane which sheds to reveal red scaly skin patches of varying sizes. Type 5 is distinguished by the location of the genetic defect - chromosome 17p13.2-p13.1.
• Navajo neurohepatopathy: A rare genetic disease found in Navajo populations. It involves peripheral nerve degeneration, liver disease and corneal ulcers. The genetic disease is believed to be caused by maternal exposure to uranium from waters contaminated by old mines.
• Nerve symptoms: Symptoms affecting the nerves
• OLEDAID: A rare syndrome characterized mainly by a weak immuned system, bone problems, lymphoedema and hair, teeth and nail abnormalities. Death usually occurs during the first few years of life due to overwhelming infections.
• Pain: Any type of pain sensation symptoms.
• Pituitary Cancer: Cancer of the pituitary gland.
• Pretibial Myxedema: Condition causing redness and thickening of soft tissues under skin and pink nodules on shins and front of lower legs; a manifestation of the autoimmune disease Graves' Disease
• Resistance to thyroid stimulating hormone: A very rare disorder where the body is unable to respond to thyroid stimulating hormone even though it is present in sufficient quantities. The problem lies in defective thyroid stimulating hormone receptors.
• Rénon-Delille syndrome: A rare syndrome characterized by reduced function of the thyroid and ovaries and enlarged hands and feet.
• Sensations: Changes to sensations or the senses
• Sick: Feeling ill or off color
• Sweat symptoms: Symptoms related to sweating
• Sweating: Sweating more than normal
• Temperature sensitivity: Changes to the body's perception of temperature
• Temperature symptoms: Abnormalities of body temperature including fever.
• Thyrotoxicosis: hypermetabolic clinical syndrome resulting from serum elevations in thyroid hormone levels, specifically free thyroxine (T4), triiodothyronine (T3), or both.
• Troell-Junet syndrome: A disorder involving enlarged extremities, diabetes, skull abnormalities and excessive thyroid hormone production.

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