El síndrome de Alagille es una enfermedad congénita y poco frecuente, se transmite de forma autosómica dominante, con expresividad variable. Se caracteriza. Alagille syndrome is an uncommon pathology. It is found in 1/, live births. It is characterized by biliary duct hypoplasia associated with. Síndrome de Alagille: una enfermedad hereditaria (genética) que provoca anomalías hepáticas y otros problemas. Deficiencia de alfa-1 antitripsina: un.

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Alagille Syndrome

At the visit, write down the name of a new enfermevad, and any new medicines, treatments, or tests. In general, be aware of the symptoms listed above.

What is alagille syndrome? Bring someone with you to help you ask questions and remember what your healthcare provider tells you. Liver biopsy Heart and blood vessel tests Eye exams Spine X-ray Abdominal ultrasound Kidney function tests Genetic testing A diagnosis of Alagille syndrome is confirmed by a liver biopsy that shows fewer bile ducts than normal and at least 3 of these symptoms: Check this box if you wish to receive a copy of your message. If you have a follow-up appointment, write down the date, time, and purpose for that visit.

A diagnosis of Alagille syndrome is confirmed by a liver biopsy that shows fewer bile ducts than normal and at least 3 of these symptoms:.

Renal manifestations in children with Alagille syndrome.

Know what to expect if you do not take the medicine or have the test or procedure. We have attempted to translate the submission below to the best of our ability through Google Translate. The documents contained in this web site are presented for information purposes only. Other blood vessels can also become smaller or unusually shaped.


Know how you can contact your healthcare provider if you have questions. Alagille syndrome is an inherited condition in which bile builds up in the liver because there are too few bile ducts to drain the bile. Ask if your condition can be treated in other ways. See all of admin’s Posts. Summary and related texts. If you do not have enough dee these ducts, bile builds up in your liver.

Mom From Cuba Describes Daughter’s Battle Against Alagille Syndrome

Changes in blood vessels. Kidneys may be smaller, contain cysts, or simply work less efficiently. Your age Your overall health and past health How sick you are How well you can handle specific medicines, procedures, or therapies How long the condition is expected to last Your opinion or preference Specific treatments for Alagille syndrome may include: Specialised Social Services Eurordis directory.

Your urine also can appear a darker color. She is an angel of Enfermesad. The following are the most common symptoms of Alagille syndrome. Other tests may be done to evaluate whether you have Alagille syndrome may include:. Privacy Policy Donate Today. Bile ducts are the channels that move bile out of your liver.

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Renal manifestations in children with Alagille syndrome.

Professionals Guidance for genetic testing Englishpdf. An enlarged spleen is more likely to be injured, especially in sports play. Contact your healthcare provider if symptoms get worse despite treatment or if new symptoms appear. Your healthcare provider will figure out the best treatment for you based on: Alagille syndrome not only affects the liver, it can also cause skin, heart, facial, kidney, and eye enfermedda.

Also know what the side effects are. Genetic testing and a discussion of the inherited risks within your family may help you make informed decisions about preventing this disease in future generations. Press f for fullscreen.

Can alagille syndrome be prevented? When to call the doctor about alagille syndrome Alagille syndrome has wide-ranging effects that may be different as the years go by and your treatment may need to be changed.

Bile is colored with a pigment called bilirubin. Key points Alagille syndrome is a genetic disorder in which you have fewer bile ducts than normal in your liver.

For all other comments, please send your remarks via contact us. It also helps digest fats and the fat-soluble vitamins A, D, E, and K.