Tag: Rare disease

Affecting less than 1 in 22,313 live births, PIK3CA-Related Overgrowth Spectrum (PROS) is a rare genetic condition. The prognosis for PIK3CA overgrowth syndrome is highly variable, depending on the severity and location of the overgrowth.

According to medical research, the duration of periodic fever syndromes is highly dependent on the specific type of condition. Understanding **how long periodic fever syndrome lasts** is a crucial aspect of managing the disease, as some resolve spontaneously while others require lifelong treatment.

A 2021 study confirmed that Dercum's disease is a rare condition in the US, affecting fewer than 200,000 individuals. Exploring **how rare is Dercum's disease** helps illuminate why its exact prevalence remains unconfirmed and often debated among medical professionals.

Affecting just 0.3% to 3% of individuals with pancreatic conditions, pancreatic panniculitis is a rare but documented complication. So, is panniculitis secondary to pancreatitis? Yes, it can be, through a complex mechanism involving pancreatic enzyme release.

With only a handful of cases reported worldwide, ALAD-Deficiency Porphyria (ADP) stands out as a candidate for **what is the rarest form of porphyria?**. This ultrarare genetic disorder is one of several types of porphyria, a group of metabolic diseases resulting from defects in the body's heme-making process.

Yes, Immune Thrombocytopenia (ITP) is considered a rare disease, with an estimated annual incidence of about 3 to 4 cases per 100,000 adults. While its rarity is clear, the perception of its frequency can differ significantly depending on the patient's age group and the form of the disease.

With an estimated 7,000 to 10,000 rare diseases identified globally, pinpointing exactly **what is the most least common disease** is a challenging and often debated topic among medical experts. Prevalence data can be elusive, and new cases of ultra-rare conditions are sometimes identified decades after the first diagnosis, shifting the rankings.

Marfan syndrome is a genetic condition affecting approximately 1 in 5,000 to 10,000 people globally, impacting connective tissue throughout the body. Given its potential to affect multiple systems, the question, **Is Marfan syndrome a big deal?**, is a crucial one for those diagnosed and their families.

Affecting an estimated 1 in 20,000 to 30,000 newborns, Poland syndrome is a rare congenital condition. Understanding **what are the chances of getting Poland syndrome** requires examining its prevalence, demographic patterns, and the largely sporadic nature of the disorder.

TTP, or Thrombotic Thrombocytopenic Purpura, is a life-threatening blood disorder with a 90% mortality rate if left untreated. But **what is TTP also known as**? This condition can be referred to by several names, depending on its specific type and the context, highlighting the importance of accurate diagnosis for effective treatment.