Waltman Walter syndrome
Waltman Walter Syndrome
Waltman Walter Syndrome (pronounced: wahl-tman wahl-ter sin-drome), also known as Dyskeratosis Congenita, is a rare genetic disorder characterized by the progressive failure of the bone marrow to produce all types of blood cells.
Etymology
The syndrome is named after the two physicians, Dr. Waltman and Dr. Walter, who first described the condition in the medical literature. The term "syndrome" is derived from the Greek word "syndromē", which means "concurrence of symptoms" or "running together".
Symptoms
The symptoms of Waltman Walter Syndrome can vary greatly among affected individuals. However, common symptoms include anemia, thrombocytopenia, and leukopenia. Other symptoms may include dyskeratosis, reticulate skin pigmentation, nail dystrophy, and oral leukoplakia.
Diagnosis
Diagnosis of Waltman Walter Syndrome is often based on the presence of characteristic signs and symptoms. Genetic testing can confirm a diagnosis in some cases. The condition is typically diagnosed through a combination of blood tests, bone marrow biopsy, and genetic testing.
Treatment
Treatment for Waltman Walter Syndrome is focused on managing the symptoms and preventing complications. This may include blood transfusions, bone marrow transplant, and medications to stimulate the bone marrow.
Prognosis
The prognosis for individuals with Waltman Walter Syndrome varies. Some individuals may have a normal lifespan with proper management, while others may have a shortened lifespan due to complications such as bone marrow failure and increased risk of cancer.
See Also
External links
- Medical encyclopedia article on Waltman Walter syndrome
- Wikipedia's article - Waltman Walter syndrome
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