Ulnar Mammary Syndrome is a rare genetic disorder caused by mutations in TBX3 and characterized by hypoplasia or aplasia of upper limbs on the ulnar side, mammary glands and nipples.
This community is for individuals with an undiagnosed medical disorder. Please post your comments, questions and symptoms in the forum section.
Unverricht-Lundborg Disease is a raregenetic epilepsy disorder.
An inflammation of the blood cells under the skin. Leaving bruising and possible swelling after an outbreak of urticarial.
Usher syndrome is a rare genetic disorder characterized by deaf-blindness due to a genetic mutation.
For those diagnosed with a mutation or deletion of the USP7 gene located on chromosome 16.
Uveitis is inflammation of the middle layer of the eye.