Doctronic Blog

Mucopolysaccharidosis Type I, or MPS I, is a rare genetic disorder that affects children. It is caused by a deficiency in an enzyme called alpha-L iduronidase, which is [...]

Nonsteroidal anti-inflammatory drugs (NSAIDs) are among the most commonly used pain relief medicines worldwide. They help alleviate headaches, sprains, arthritis symptoms, [...]

Pick's disease is a rare form of dementia that affects the frontal and temporal lobes of the brain, which control emotions, behavior, personality, and language. It is a [...]

Peripheral artery disease (PAD) is a condition in which your arteries become narrowed, reducing blood flow to your limbs. It's a form of peripheral vascular disease that [...]

Pfeiffer syndrome is a rare genetic disorder that affects the development of a baby's skull and face. This condition causes the skull bones to fuse too early, preventing [...]

Trisomy 13, also known as Patau syndrome, is a rare genetic condition that occurs when a baby has an extra 13th chromosome. This extra genetic material disrupts the [...]

Infantile spasms, also known as West syndrome, is a rare type of seizure disorder that affects babies. If your baby has been diagnosed with infantile spasms, it's [...]

Rapp-Hodgkin syndrome is a rare genetic disorder that affects various parts of the body, including hair, nails, skin, sweat glands, and teeth. It is part of a larger group of [...]

Short Bowel Syndrome (SBS) is a condition that affects people who have had a significant portion of their small intestine removed or are born with a shorter small intestine. [...]

Endometriosis is a chronic condition that requires a long-term management plan tailored to the extent of the disease, severity of pain, and your potential plans for [...]