Doctors said that the 46-year-old Hussein Ali Radhi suffers from Achondroplasia, a genetic disorder which he acquired due to his mother's excessive consumption of chewing gum during her pregnancy.
The presence of Thalidomide in the chewing gums caused Hussein to develop the genetic problem, also known as the Seal Syndrome, doctors said.
"Considering his small body size, it was a challenge to reach his coronary artery. Usually angiography is done from right femoral artery that is in right groin or radial artery in the right wrist," said Dr Viveka Kumar, Director-Cardiac Cath Labs and senior consultant, Interventional Cardiology and Electrophysiology at Max Hospital, where Hussein underwent treatment.
Hussein had started feeling angina and breathlessness due to exertion. He consulted many doctors in Iraq but, due to his structural abnormality, they could not perform an angiography on him as the coronary artery was inaccessible.
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He then turned to India and admitted himself at the super speciality hospital in Saket on May 31.
After diagnosis, doctors there found that his two arteries were blocked, leading to the pain and breathlessness. Since his arms were very small, the arteries were bent and tortuous, they said.
"This is a first-of-its-kind (operation) in the literature of multi-vessel PTCA (Percutaneous Transluminal Coronary Angioplasty), in an Achondroplasia patient with fixed deformity and severe shortening of both upper and lower limbs," said Kumar.
Hussein was discharged on June 2. He is in hale and hearty condition and will get back to his hometown soon, doctors said.