Share on FacebookIndian doctors are working tirelessly to uncover the mystery behind an 18-month-old girl's extraordinary weight. Aliya Saleem has grown to a staggering 53 pounds—more than double the weight of an average child her age—and her condition is causing concern and financial strain for her family.
A Rare Medical Mystery
Dr. Bhavya Kumar, a leading physician, suspects that Aliya may have Prader-Willi Syndrome, a rare genetic disorder. This condition is known to cause learning challenges, abnormal growth patterns, and an insatiable appetite.
“There could be a hormonal imbalance, a metabolic disease, or genetic causes,” Dr. Kumar shared. “I strongly suspect this is a rare genetic disorder.”
Medical experts are continuing their tests to confirm the diagnosis, hoping to better understand what is behind Aliya's rapid weight gain.
A Family's Struggle
Aliya's parents, Shabnam Parveen and Mohammad Saleem, are doing everything they can to provide for their daughter. With a 5-year-old son of average weight, the couple wasn’t prepared for the unique challenges Aliya’s condition would bring.
“She eats about three times more than other kids her age,” Shabnam explained. “If we don’t feed her, she cries endlessly and becomes very upset.”
Mohammad, a tailor who earns only $3 a day, faces immense pressure to keep up with his daughter's needs. The family spends nearly all their income on food for Aliya.
The Hidden Costs of Growth
Aliya's appetite isn't the only challenge. Her rapid weight gain means she outgrows her clothes every two weeks, further straining the family's limited resources.
“Her constant hunger leads to excessive weight gain,” Shabnam said. “We are always buying her new clothes, and it’s becoming too much for us to manage.”
Seeking Hope and Answers
For now, the family continues to search for answers and hope that doctors can provide a clear diagnosis and effective treatment plan for Aliya. While they wait, they face the daily challenge of balancing their love and care for their daughter with the financial reality of their situation.
This extraordinary case highlights the struggles many families face when caring for children with rare medical conditions—and the strength it takes to keep going.
