Alagille syndrome
Overview
Alagille syndrome is a genetic disorder that affects the liver, heart, and other systems of the body. Problems associated with the disorder generally become evident in infancy or early childhood.
Alagille Syndrome
Alagille syndrome has been recognized since the 1970’s and was first reported as a syndromic form of liver disease. Cases have been found from around the world although it is a relatively rare inherited disorder.
Alagille syndrome is a genetic disorder that causes a loss of bile ducts in the liver and narrowing of the ducts outside the liver. The resulting buildup of bile in the liver can cause scarring and cirrhosis.
Alagille syndrome
Disease Information
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Alagille Syndrome
National Organization for Rare Disorders, Inc.
Synonyms ...
Alagille Syndrome
By Sonja Rene EubanksThomson Gale, Gale.. Gale Encyclopedia of Genetic Disorders Part II, 2005more »
Definition ...
Can Alagille syndrome be inherited?
This condition is inherited in an autosomal dominant pattern, which means one copy of the altered or deleted gene in each cell is sufficient to cause the disorder.
How is Alagille syndrome diagnosed?
Because the symptoms of Alagille syndrome vary and because the syndrome is so rare, the disorder can be difficult to diagnose.
Alagille Syndrome Symptoms, Diagnosis, Treatments and Causes - WrongDiagnosis.com
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Alagille Syndrome ...
Alagille Syndrome
Alagille-Watson syndrome
Alan's Story: Coping With Change After a Heart Attack
Albers-Schonberg Disease
Albinism with Hemorrhagic Diathesis and Pigmented Reticuloendothelial Cells
Albinism, ocular
Albinism, Oculocutaneous ...
Ductular hypoplasia, syndromatic hepatic: Also called Alagille syndrome or arteriohepatic dysplasia, this is a genetic disorder characterized by jaundice in the newborn period, liver disease with cholestasis, ...
Alagille Syndrome: A genetic disorder affecting the liver and characterized by the absence of some or all of the liver bile ducts that transport bile within the liver.
: Alagille syndrome and nephroblastoma: Unusual coincidence of two rare disorders. Pediatr Blood Cancer 50 (4): 908-11, 2008.
Scott RH, Walker L, Olsen ØE, et al.
In the syndromic type (see Alagille syndrome) vertebral body abnormalities, which include butterfly and hemivertebra are present characteristically in the Thoracic: Relating to the thorax, ...
Alagille Syndrome
Alan's Story: Coping With Change After a Heart Attack
Alanine Aminotransferase (ALT) - Medical Test
Albendazole for the treatment of pinworms - Medication
Albers-Schonberg Disease ...
Peripheral pulmonary stenosis with cholestasis: Also known as arteriohepatic dysplasia or Alagille syndrome, this ia a genetic disorder characterized by jaundice in the newborn period, liver disease with cholestasis, ...
alagille syndrome, a condition in which the bile ducts narrow and deteriorate, especially during the first year of life
alpha 1- antitrypsin deficiency, a genetic liver disease in children that can lead to hepatitis and cirrhosis of the liver ...
Adrenogenital Syndrome; Alagille Syndrome; American Geriatrics Society; Audiogenic Seizures
AHA ...
Vatan Hastanesi Aksoy Hastanesi Aktob AKU Al Ahmadi Al Dukair Al Hada and Taif Military Hospitals Al Jazira Clinic Al Mana General Al Mouwasat General Al Rawdah Al Yousif Al-hijamah Al-Mana Ala ALA Ala-cort Ala-scalp Alactasia Alagille syndrome ...
(Duodenal atresia) - Imperforate anus - Meckel's diverticulum - Hirschsprung's disease - Intestinal malrotation - Persistent cloaca
Pancreas
Annular pancreas - Accessory pancreas - Pancreas divisum
Other
Choledochal cysts - Alagille syndrome ...
 See also: Symptom, Diabetes, Kidney, Autosomal dominant, Dysplasia
  
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