Suffering from uncommon diseases, do not lose hope!
Ankita Chakrabarty/ Zee Research Group/ Delhi
How did you react when you saw Big B as ‘Auro’ in the movie ‘Paa’? You must be bewildered or curious to know as to how a 12 –year old child can look like a 70 year old man? It was because Amitabh was suffering from a rare genetic disorder called ‘progeria’.
Rare or uncommon diseases do not only exist in reel life but also in real life; a recent case of this is of the 16-month-old girl from Tripura, who is suffering from Hydrocephalus, a condition in which cerebrospinal fluid builds up in the brain and causes swelling. She is now in the capital to seek treatment.
Rarest diseases have always been the centre of discussion among the medical fraternity but the general public was not earlier aware given the very low penetration.
The medical fraternity is of opinion that the diagnostic modalities are getting improved and are easily accessible in India. Dr. Vandana Kent, senior consultant at Rockland Hospital, says, “Uncommon diseases are not at all becoming common in India, it is just that the state of education in our country and the technology has made the people more aware about the existence of such diseases.”
Some examples of the rarest of rare diseases in India which have caught the attention of public in recent past are Progeria, Congenital Insensitivity to pain with anhidrosis (CIPA) and conjoint twins.
Progeria is a rare abnormality and causes premature ageing in the children. In India, there is one case of progeria in a family. According to media reports, in the state of Bihar, Bisul Khan and his wife Razia Khatoon have a total of seven children of which five are suffering from progeria.
According to Progeria Research Foundation (http://www.progeriaresearch.org/), Progeria affects approximately one in four - eight million newborns. There are an estimated 200-250 children living with Progeria worldwide at any one time. Progeria signs include growth failure, loss of body fat and hair, aged-looking skin and stiffness of joints.
Congenital insensitivity to pain with anhidrosis or CIPA is an inherited disease of the nervous system that prevents the sensation of pain, heat, cold, or any real nerve-related sensations. It is also one of the rarest of its kind, with the first case being reported in 1983. In India, till date two cases have been reported.
According to facts provided by University of Maryland Medical Center (http://www.umm.edu/), conjoined twins are genetically identical, and are, therefore, always the same sex. They develop from the same fertilized egg, and they share the same amniotic cavity and placenta. Approximately 40 to 60 percent of conjoined twins arrive stillborn, and about 35 percent survive only one day. The overall survival rate of conjoined twins is somewhere between five – 25 percent.
The Indian Healthcare system has notched up several significant achievements over the last 50 years in dealing with the uncommon diseases. Dr. Sandeep Vaishya, additional director, neurosurgery at Fortis Memorial Research Institute, Gurgaon, says, “India is fully equipped and technologically advanced to treat such diseases. All this requires skilled clinical expertise, trained physicians, technological advancements and infrastructure to go for certain complex surgeries which are available nowadays.”
Earlier this month the court refused the option of a surgery to separate Saba and Farah and directed the state government to grant the family Rupees 5, 000 per month. Saba and Farah are conjoined twins and they share an artery that carries blood to their hearts. Also, Farah has two kidneys while Saba has none.
“Access to medical care at right time is important for the treatment of such kinds of rare diseases,” warns Dr. Srikant Sharma, consultant, internal medicine at Moolchand Medcity, New Delhi.
Hope prevails for those unlucky who are born with an uncommon disease.
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