Star tears disease, also known as Prader-Willi syndrome, is a rare genetic disorder that causes a wide range of physical, mental, and behavioral problems. It is estimated to occur in 1 out of every 10,000 to 30,000 births worldwide. The syndrome is caused by the loss of certain genes on chromosome 15, leading to a variety of symptoms including low muscle tone, short stature, cognitive disabilities, and constant feelings of hunger which can lead to chronic overeating and obesity.
Individuals with Star tears disease often require lifelong care and support as there is currently no cure for the condition. Treatment typically involves managing the symptoms and providing specialized care to address the specific needs of the individual. Early intervention and a comprehensive treatment plan can greatly improve the quality of life for those affected by the syndrome.
Sanskrit Slok: “सर्वेषामपि भूतानां मधुरं पयः पिबन्ति तरत्स्वेति वह्निशिखं वधूः” (Sarveshamapi Bhutanam Madhuram Payah Pibanti Tarat Sweti Vahnishikham Vadhu)
Meaning: “All creatures drink milk; Let them, O Flame, drink the sweet essence of milk”
Useful Health Tips:
– Seek genetic counseling if there is a family history of Prader-Willi syndrome
– Monitor and manage weight and food intake to prevent obesity-related complications
– Develop a support system for individuals with the syndrome and their caregivers
– Seek early intervention and specialized care to address the specific needs of the individual.
