Bardet-Biedl syndrome, type 1

Below you will find more information about Bardet-Biedl syndrome, type 1 from Medigest. If you believe that you are suffering from any of the symptoms of Bardet-Biedl syndrome, type 1 it is important that you obtain an accurate diagnosis from a medical professional to ensure that you obtain the correct medication or treatment for your condition. There are medical conditions that carry similar symptoms associated with Bardet-Biedl syndrome, type 1 and therefore the information provided by Medigest is offered as a guideline only and should never be used in preference to seeking professional medical advice. The information relating to Bardet-Biedl syndrome, type 1 comes from a third party source and Medigest will not be held liable for any inaccuracies relating to the information shown.


Bardet-Biedl syndrome, type 1 is an unusual hereditary or genetic disorder distinguished by mental retardation, polydactyly, obesity and pigmentation of the retina and other anomalies. Bardet-Biedl syndrome, type 1 results from the deficiency in chromosome 11q13.


Bardet-Biedl syndrome, type 1 is classified as a "rare disease" according to the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH) which means that it affects not more than 200,000 individuals in the US population.

Symptoms and Signs

The list below is the known symptoms of Bardet-Biedl syndrome, type 1: Obesity Short stature Mental deficiency Low verbal I.Q. Low performance or I.Q. Inappropriate mannerisms Visual impairment Retinal dystrophy Myopia Astigmatism Nystagmus Glaucoma Cataracts Aphakia Retinitis pigmentosa Take note that the symptoms might not be seen by patients but by physicians or medical experts.


The list below is the known complications experienced by individuals affected by Bardet-Biedl syndrome, type 1: Blindness Renal failure

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