Tag: Rare condition

Affecting an estimated 50 to 300 people per million, systemic sclerosis (SSc), also known as scleroderma, is a rare autoimmune disease that attacks the internal organs by causing an overproduction of collagen. This condition can lead to widespread scarring and thickening (fibrosis) that can severely impact organ function and quality of life.

Fewer than 3,000 people in the United States are diagnosed with AL amyloidosis annually, a rare and serious blood-related disorder. This condition, a form of systemic amyloidosis, occurs when the body's plasma cells produce abnormal proteins that form harmful deposits throughout the body. Knowing what is the blood disease AL amyloidosis is the first step toward understanding its impact and navigating treatment options.

With fewer than 400 cases reported worldwide, Urbach-Wiethe disease (UWD) is an extremely rare genetic condition. Often mistakenly referred to as the **Urban Wiethe syndrome**, it is an autosomal recessive disorder that affects the skin, mucous membranes, and internal organs due to the deposition of hyaline-like material.

According to the National Institutes of Health, Poland syndrome is a rare congenital disorder affecting approximately 1 in 20,000 newborns. This condition is the primary answer to the question: can you be born without a pectoral muscle?, as it involves the absence or underdevelopment of the chest wall muscles on one side of the body.

Statistics indicate that Superior Mesenteric Artery Syndrome (SMAS) has a worldwide incidence of just 0.1-0.3%, confirming that **is SMAS a rare disease?** Yes, it is. This is a severe but often overlooked gastrointestinal condition that results from anatomical compression of the small intestine.

Madelung's disease, also known as multiple symmetric lipomatosis (MSL), is a rare disorder characterized by the symmetrical growth of benign fat deposits around the upper body. Recognizing the key signs is the first step, so how do I know if I have Madelung's disease and not another condition?

Trichobezoar is an extremely rare condition, occurring in less than 1% of the general population and less than 6% of all bezoar cases. The vast majority of diagnoses are found in young females under 30 who suffer from underlying psychiatric conditions. Despite its infrequency, understanding this hairball formation is crucial for timely diagnosis and management.

The complete absence of a heart at birth is a medical condition known as acardia, and it is a rare phenomenon primarily associated with identical twin pregnancies, rather than a viable single birth. Independent survival without a functioning heart is not possible.

Ascher's syndrome, a rare and benign disorder, was first identified by an ophthalmologist in 1920. This condition is primarily defined by a classic triad of symptoms, but not all patients present with all three. Understanding **what is Ascher's syndrome symptoms** is crucial for accurate diagnosis, as it can often be misdiagnosed due to its rarity.

Did you know there are fewer than 300 reported cases of Urbach-Wiethe disease in medical literature? The question of **how to get Urbach-Wiethe disease?** is based on a fundamental misunderstanding, as this rare condition is not something you can acquire or contract, but an inherited genetic disorder.