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Patient Testimonial for Noonan Syndrome with Cyanotic Congenital Heart Disease

Testimonial by Mast. Vincent Mbaiwa

Treatment for: Noonan Syndrome with Cyanotic Congenital Heart Disease
Treated by: Dr. P. V. Naresh Kumar
Speciality:
Patient location: Zambia

Noonan syndrome is caused by a defective gene, which may impair the normal development of various body parts. Along with probable developmental delays, this genetic condition can cause low stature, heart disorders, odd facial characteristics, short stature, and other physical issues.

Cyanotic congenital heart disease is a condition in which numerous cardiac abnormalities are present at birth (congenital), resulting in low blood oxygen levels. The term “cyanosis” describes the bluish hue of the mucous membrane and skin. Tetralogy of Fallot, TGA, TAPVC, truncus, and anomalies of the tricuspid valve are a few examples of prevalent cyanotic congenital heart disease.

Depending on the severity of the symptoms, cyanotic congenital heart disease treatment may or may not be required. Some types of heart issues may be successfully treated by specific medications. In many instances, surgery is ultimately required to fix the structural flaws in the heart. Oxygen therapy and surgery to correct the abnormalities or reroute blood flow are among the available treatments. A regular assessment of cardiac function may also be advised by the physician.

It can take eight to twelve weeks for the child’s chest wound to heal completely (for the stability of the sternum). A dressing will be applied to the wound and will remain in place for around two weeks after surgery. At least 3 or 4 more weeks will be required for the child to heal at home. Recovery from major surgery could take 6 to 8 weeks.

Mast. Simwalu Lubuto from Zambia, underwent treatment for Noonan Syndrome with Cyanotic Congenital Heart Disease, under the supervision of Dr. P. V. Naresh Kumar, Consultant Cardiothoracic & Transplant Surgeon, Yashoda Hospitals, Hyderabad.

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