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Bardet-Biedl syndrome 1

Der BBS1 gene provides instructions for making a protein found in cells throughout the body. The BBS1 protein is part of a group (complex) of proteins that plays a critical role in the formation of cell structures called cilia. Cilia are microscopic, finger-like projections that stick out from the surface of many types of cells. They are involved in cell movement and many different chemical signaling pathways. Cilia are also necessary for the perception of sensory input (such as sight, hearing, and smell).

Normal function

Der BBS1 gene provides instructions for making a protein found in cells throughout the body. The BBS1 protein is part of a group (complex) of proteins that plays a critical role in the formation of cell structures called cilia. Cilia are microscopic, finger-like projections that stick out from the surface of many types of cells. They are involved in cell movement and many different chemical signaling pathways. Cilia are also necessary for the perception of sensory input (such as sight, hearing, and smell).

Conditions referring to this gene or chromosome

Other names

BBS1_HUMAN

BBS2L2

FLJ23590

Related patient information and medicines

Alpha-1-Antitrypsin-Mangel

Patient information leaflet

Alpha-1-Antitrypsin-Mangel

A special test known as a phenotype test can show the gene variation that a person has. People who have two copies of the Z-type faulty gene produce the least amount of normal A1AT and are most severely affected. How common is alpha-1 antitrypsin deficiency. Between 1 in every 3,000 to 5,000 people in the UK haben A1AT deficiency. Around 1 in 30.

6-in-1-Impfstoff

Patient information leaflet

6-in-1-Impfstoff

The 6-in-1 vaccine used to be given as the 3-in-1 vaccine DTaP along with the polio vaccine which was given by mouth, but has gradually been extended so that it now protects against even more diseases. It is given in one single injection into the thigh from one single syringe. This leaflet explains when this Impfstoff is given and why. It also.

Down-Syndrom

Patient information leaflet

Down-Syndrom

Down's syndrome (also known as Down syndrome) ist a genetic chromosome problem. Someone with Down's syndrome has an extra copy of chromosome 21 in the cells of their body. All people with Down's syndrome have some degree of learning disability. Down's syndrome may be detected before birth (prenatally) or after birth (postnatally). It cannot be.

Halsrippe

Patient information leaflet

Halsrippe

About 1 in 100 people are born with an extra rib called a cervical rib. About 1 in 10 people who have a cervical rib develop thoracic outlet syndrome. This happens if the cervical rib squashes the nerves and blood vessels going into the arm. Treatment can include painkillers, physiotherapy and sometimes surgery to relieve the compression caused.

Mikrovaskuläre Angina

Patient information leaflet

Mikrovaskuläre Angina

Es gibt no agreed definition for CSX. The underlying cause may be sudden narrowing (spasm) of normal coronary arteries without any evidence of atheromatous fatty plaques. What is cardiac syndrome X. Cardiac syndrome X (CSX) is thought to be a type of angina. In CSX chest pain is felt when the heart works harder but the heart arteries appear to be.

Typ-1-Diabetes

Patient information leaflet

Typ-1-Diabetes

Typ-1-Diabetes ist the type of diabetes that typically develops in children and in young adults. In type 1 diabetes the body stops making insulin and the blood sugar (glucose) level goes very high. Treatment to control the blood glucose level is with insulin injections and a healthy diet. They include reducing blood pressure if it is high and.

Weiterführende Lektüre und Referenzen

Artikelverlauf

Die Informationen auf dieser Seite werden von qualifizierten Klinikern verfasst und begutachtet.
  • 18. Aug 2020 | Neueste Version
  • 1 May 2010 | Ursprünglich veröffentlicht

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