Journal of Law and Genetics

Marfan syndrome - symptoms and breakthroughs Marfan syndrome is a genetic disorder affecting cognitive tissue. Marfan syndrome affects may organs such as the heart, eyes, blood vessels and skeleton. Typically, people with Marfan syndrome are tall and thin with long limbs, including fingers. The symptoms and complications of Marfan syndrome vary from person to person.

A client was deceived by a Solicitor without a practicing certificate, who accepted money to pursue an appeal and then did not complete the work. Gavin Clarke’s behavior was described as “fundamentally incompatible’ with continued membership of the profession by the Solicitor’s Disciplinary Tribunal and he has now been struck off.

Turner syndrome (TS), also known as Ullrich-Turner syndrome, is a rare chromosomal condition that affects females only. It occurs when one of the two X chromosomes is missing or partially missing. It affects 1 in 2,000 female births worldwide. About 50% of those with Turner Syndrome have only one X chromosome, some have complete X chromosome and one partially missing or rearranged X chromosome.