Syndrome
Syndrome , Klippel-Trenaunay-Weber (KTW): A congenital malformation
syndrome characterized by the triad of asymmetric limb hypertrophy , hemangioma ta, and nevi.
Syndrome : A set of signs and symptoms that tend to occur together and which reflect the presence of a particular disease ...
Aarskog syndrome
Aarskog
Syndrome Aase
Syndrome Aase-Smith
Syndrome (Aase
Syndrome ) AAT Deficiency ( Alpha-1 Antitrypsin Deficiency ) A bacterial Cystitis ( Cystitis - Noninfectious ( Acute Urethra l
Syndrome )) ... Like many minor anatomic variations, a single transverse palmar crease is associ...
Acquired Immunodeficiency Syndrome
ACQUIRED IMMUNODEFICIENCY
SYNDROME - A fatal disease that destroys the host 's immune system resulting from infection with human immuno deficiency virus ( HIV ). [ Med Help International ] [ Search ] [ Ask the Doctor Forums ] ... illnesses of the brain (neurological) and nerve s, bo...
Acute nephritic syndrome
Acute nephritic
syndrome Definition: Acute nephritic
syndrome is a group of disorders that cause inflammation of the internal kidney structures (specifically, the glomeruli). Acute nephritic
syndrome is the result of inflammation of the internal structures of the kidney , often caus...
Alport syndrome
Alport
syndrome Dr Trisha Macnair Dr Trisha Macnair Those affected by alport
syndrome develop progressive loss of renal ( kidney ) function, and sometimes progressive deafness and abnormalities of the eye . Alport
syndrome is very similar to hereditary nephritis . There may be nerve...
Angelman Syndrome
Angelman
syndrome : An important genetic
syndrome characterized by severe motor and intellectual retardation , microcephaly (abnormally small head), ataxia , frequent jerky limb movement s and flapping of the arms and hands, hypotonia (floppiness), ... Angelman
syndrome (AS) is a...
Aortic arch syndrome
Aortic arch
syndrome Definition: The aorta is the large, main artery carrying blood away from the heart . Subareolar Abscess Subclavian Artery Occlusive
Syndrome ( Aortic Arch
Syndrome ) Subclavian Steal
Syndrome ( Aortic Arch
Syndrome ) Subconjunctival Hemorrhage Subcutaneou...
Apert syndrome
Apert
syndrome Dr Trisha Macnair Some genetic conditions lie hidden away deep within the cells, causing mischief that may not be very apparent, at least until later in life. Apert
Syndrome Aphthous Ulcer ( Canker Sores ) Apo lipoprotein B Deficiency (Bassen-Kornzweig
Syndrome ) Apop...
Battered child syndrome
Battered child
syndrome ; Physical abuse - children Prevention : Recognize the warning signs of potential abuse . These include when the caregiver: ... Bathing Trunk Nevus Batten Disease ( Neuron al Ceroid Lipofuscin oses (NCLS)) Battered Child
Syndrome B- Cell Lymphoma ( Burki...
Carcinoid syndrome
Carcinoid
syndrome . This
syndrome is a combination of signs and symptoms, including flushing of the skin and diarrhea . Carcinoid
syndrome -- a disease caused by abnormal cells of the lungs and gut which produce hormone s Thyroid storm -- a condition caused by excessive production ...
Carpal tunnel syndrome
Carpal tunnel
syndrome is becoming more frequently recognized and may be occurring more often. It may result from repetitive motion or the use of devices like computer keyboards. Carpal tunnel
syndrome What is Carpal Tunnel
Syndrome ? Carpal Tunnel
Syndrome (CTS) is a condition that caus...
Chronic Fatigue Syndrome
Chronic fatigue
syndrome : A debilitating and complex disorder characterized by profound fatigue of six months or longer duration that is not improved by bed rest and that may be worsened by physical or mental activity. Chronic fatigue
syndrome Definition: Chronic fatigue
syndrome is a co...
Cockayne Syndrome
Cockayne
syndrome Bjorn pili torti and deafness
syndrome Multi ple synostosis
syndrome Hunter
syndrome Taybi oto-palato- digit al
syndrome Hereditary nephritis Mohr
syndrome Hurler
syndrome Waardenburg
syndrome Kartagener
syndrome ... Cockayne
syndrome Bjorn pili...
Compartment syndrome
Compartment
syndrome Definition: Compartment
syndrome involves the compress ion of nerve s and blood vessels within an enclosed space. This leads to impaired blood flow and muscle and nerve damage. Compartment
syndrome All muscle s are surrounded by a protective sheath and somet...
Cornelia De Lange Syndrome
Cornelia de Lange
syndrome Dr Trisha Macnair There's still much to learn about this rare condition, which can cause a range of mild to severe symptoms. We look at its effects, the possible causes and where you can find support. It is also associated with
syndrome s without a familial inherita...
Crest syndrome
CREST
syndrome is a subset of scleroderma , a disorder that leads to thickening, hardening and tightening of your skin and connective tissue . CREST
syndrome : A limited form of scleroderma , a disease of connective tissue with the formation of scar tissue (fibrosis) in the skin...
Crigler-Najjar Syndrome
Crigler-Najjar
syndrome Definition: Crigler-Najjar
syndrome is an inherited disorder in which bilirubin (a substance made by the liver ) cannot be changed into its water-soluble form, bilirubin glucuronide. Arias
Syndrome (Type II Crigler-Najjar) ( Crigler-Najjar
Syndrome ) Arkless-Gr...
DiGeorge Syndrome
DiGeorge
syndrome affects about one in 4,000 birth s DiGeorge
syndrome affects about one in 4,000 birth s. Most cases result from a deletion of a tiny part of chromosome 22 known as 22q11.2 (the DiGeorge
syndrome chromosome region, or DGCR). DiGeorge
syndrome is a childhood disea...
Down syndrome
Down
syndrome is a genetic disorder that includes a combination of birth defects , including some degree of mental retardation , characteristic facial features and, often, heart defects, visual and hearing impairment , and other health problems. Down
syndrome occurs in about one in ev...
Dubin-Johnson syndrome
DUB (Dysfunctional Uterine Bleeding (DUB)) Dubin-Johnson
Syndrome Duchenne Muscular Dystrophy Duhring's Disease ( Dermatitis Herpetiformis) Duodenal Atresia ... disorders present since birth that cause problems processing bilirubin (Gilbert's
syndrome , Dubin-Johnson
syndrome ...
Ehlers-Danlos syndrome
Ehlers-Danlos
syndrome Prevention : Genetic counseling is recommended for prospective parents with a family history of Ehlers-Danlos
syndrome . Affected parents should be aware of the type of Ehlers-Danlos
syndrome they have and its mode of inheritance. Ehlers-Danlos
syndrome is relati...
Empty sella syndrome
Empty sella
syndrome Definition: Empty sella
syndrome is the absence of the pituitary gland on radiological im aging of the sella turcica, a bony structure that normally partly surrounds the gland . incentive plans; employee performance appraisal; employee retirement income security act;...
Fatigue Syndrome
Chronic fatigue
syndrome is a complicated illness characterized by at least six months of extreme fatigue that is not relieved by rest, and a group of additional symptoms that also are constant for at least six months. Chronic Fatigue
Syndrome Related Category: Pathology (CFS), colle...
Fragile X syndrome
Fragile X
syndrome is the most common form of inherited mental retardation in males and a significant cause in females. The inheritance is different from common dominant or recessive inheritance patterns. Fragile X
syndrome Dr Trisha Macnair Fragile X
syndrome (or Martin-Bell
syndrome )...
Guillain-barre Syndrome
Guillain-Barre
syndrome Definition: Guillain-Barre
syndrome is a disorder caused by nerve inflammation involving progressive muscle weakness or paralysis , which often follows an infectious illness. Doctors and scientists don't know what causes Guillain-Barre
syndrome . However, th...
HELLP syndrome
HELLP
Syndrome ...A Pregnancy Complication What is the HELLP
syndrome ? The answer is in the MedicineNet Medical Dictionary. The entry there reads: ... HELLP
syndrome : A
syndrome featuring a combination of "H" for hemolysis (the breakdown of red blood cells), "EL" for elevated liver...
Hepatorenal syndrome
Hepatorenal
syndrome Definition: Hepatorenal
syndrome is acute kidney failure occurring without other cause in a person with severe liver disease . Hepatorenal
syndrome occurs when there is a decrease in kidney function in a person with a liver disorder. The most common symptom is d...
Hunter syndrome
MPS disease s include Hurler
syndrome , Scheie
syndrome , Hurler- Scheie
syndrome , Hunter
syndrome , Sanfilippo
syndrome (types A, B, C and D), Morquio, Maroteaux Lamy
syndrome , Sly
syndrome and MPS IX. The sole exception to autosomal recessive inheritance is MPS type II ( Hunter sy...
Hurler syndrome
Hurler
syndrome Definition: Hurler
syndrome is an inherited disease that belongs to a group of disease s called mucopolysaccharidoses, or MPS. Hurler
Syndrome HUS ( Hemolytic -Uremic
Syndrome ( HUS )) Hutchinson Incisor s ( Tooth - Abnormal Shape) Hutchinson-Gilford
Syndrome (Pr...
Infant Respiratory Distress Syndrome
Infant Respiratory Distress
Syndrome Related Category: Pathology ( IRDS ) or hyaline membrane disease (h´ln, -ln´´), respiratory di stress
syndrome of newborns, ... IRDS ( Infant Respiratory Distress
Syndrome ) Iritis ( Uveitis ) Iron Deficiency Anemia Iron Defici...
Klinefelter syndrome
Klinefelter
syndrome Definition: Klinefelter
syndrome is a condition that occurs in men as a result of an extra X chromosome . The most common symptom is infertility . Klinefelter
Syndrome Klippel-Trenaunay
Syndrome Klippel-Trenaunay-Weber
Syndrome (Klippel-Trenaunay
Syndrome ) Klum...
Lambert-Eaton Syndrome
LAMBERT-EATON
SYNDROME - A condition characterized by muscle weakness that is similar to the symptoms of myasthenia gravis . For this reason, it has been referred to as myasthenic
syndrome . Lambert-Eaton
syndrome and myasthenia gravis also have symptoms that may be similar to early ...
Marfan syndrome
Marfan
syndrome Definition Marfan
syndrome is an inherited disorder of the connective tissue that causes abnormalities of the patient's eyes , cardiovascular system, and musculo skeletal system. Marfan
syndrome Symptoms: Family history of Marfan
syndrome Long, lanky frame Long, thi...
Milk-alkali syndrome
Milia ry Tuberculosis (Disseminated Tuberculosis ) Milk Intolerance ( Lactose Intolerance ) Milk-Alkali
Syndrome Mimic Spasm (Facial Tics ) Minamata Bay Disease (Methyl mercury Poisoning ) ... Elevations may be seen in hyperparathyroidism , metastatic bone tumor , milk-alkali syn...
Morquio syndrome
Morquio
syndrome Definition: Morquio
syndrome is an inherited disease belonging to the group of mucopolysaccharide storage disease s. Two forms are recognized, type A and type B. Mucopolysaccharidosis Type IVA (Galactosamine-6-Sulfatase Deficiency ) ( Morquio
Syndrome ) Mucopolysaccharid...
Munchausen Syndrome
Munchausen
syndrome is a rare but serious condition in which a person tries to appear sick or injured in order to get attention. Doctors may also refer to this as factitious disorder. Munchausen
syndrome by proxy Definition: Munchausen
syndrome by proxy is a form of child abuse in which ...
Nephrotic syndrome
Nephrotic
Syndrome in Adults Nephrotic
syndrome is a condition marked by very high levels of protein in the urine ( proteinuria ); low levels of protein in the blood ; swelling , especially around the eyes , feet, and hands; and high cholesterol . Nephrotic
syndrome is characteri...
Noonan syndrome
Noonan
syndrome can be inherited in an autosomal dominant manner. It affects at least 1 in 2,500 children. Noonan
syndrome may result from excessive SHP-2 activity. Typical features include abnormalities of the heart . NS: Noonan
syndrome , a multi faceted condition characterized by ...
Opitz Syndrome
Smith-Lemli- Opitz
syndrome : A multi ple congenital malformation
syndrome caused by an abnormality in cholesterol metabolism , deficiency of the enzyme 7-dehydro cholesterol reductase (DHCR7), due to mutation of the DHCR7 gene on chromosome 11. a number of different dysmorphi...
Organic brain syndrome
Organic brain
syndrome Definition: Organic brain
syndrome is a general term referring to physical disorders (usually not psychiatric disorders) that cause decreased mental function. Organic brain
syndrome : Psychiatric or neurological symptoms, including problems with attention, concentrati...