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Infantile Hypophosphatasia

Infantile Hypophosphatasia: A family of children diagnosed with the rarest of diseases — Infantile Hypophosphatasia struggling to get these genetic disorders included under the Centre’s National Policy for Rare Diseases (NPRD). Infantile Hypophosphatasia is a rare genetic disease in which the patient’s bones and teeth demineralise, making her fragile and prone to fractures. It may […]

Guillain-Barre Syndrome : Recent study

Guillain-Barre Syndrome : Recent study In a recent study from Israel, a connection was found between Covid-19 infection and a higher likelihood of being diagnosed with Guillain-Barre syndrome (GBS) within six weeks. Guillain-Barre syndrome is a rare autoimmune disorder where the body’s immune system mistakenly attacks the peripheral nerves. It is more common in adults […]

Reversible Inhibition Of Sperm Under Guidance

Reversible Inhibition Of Sperm Under Guidance: The Indian Council of Medical Research (ICMR) has successfully tested a long-lasting male contraceptive called “Reversible Inhibition of Sperm Under Guidance” (RISUG). RISUG is a non-hormonal injectable male contraceptive that blocks the production of sperm by creating a physical barrier in the vas deferens, the tube that carries sperm. […]

Niemann-Pick Disease

Niemann-Pick Disease: Parents of children suffering from Niemann-Pick disease have urged the Union government to notify the ailment under the National Policy for Rare Diseases. Niemann-Pick Disease is a rare genetic disorder in which sphingomyelin accumulate in lysosomes inside cells. This disease involves dysfunctional metabolism of sphingolipids. The three most commonly recognized forms are Niemann-Pick […]