How long can you live with Diamond Blackfan Anemia?

What are the survival rates of Diamond Blackfan anemia? Children with DBA can live long lives with treatments. Some people treated for DBA achieve complete remission and do not need treatment, meaning their symptoms go away for more than six months. This can last for years and can become permanent.

How many cases of Diamond Blackfan anemia are there?

Diamond Blackfan anemia affects approximately 5 to 7 people per million live births per year. Thus in the United States, with 4 million livebirths per year, there are approximately 25-35 new patients born per year. There are several approximately 5000 cases world-wide.

Is Diamond Blackfan Anemia genetic?

This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. In approximately 45 percent of cases, an affected person inherits the mutation from one affected parent .

Is DBA fatal?

Treatments. Children diagnosed with DBA are able to live long lives with medical treatment. And some go into complete remission, meaning the symptoms disappear for a time. Two common treatments are blood transfusion therapy and corticosteroid medication.

Who is Audrey nethery?

Audrey Nethery, 6-year-old girl with a bone marrow disease, is Zumba sensation. At a Zumba convention in Orlando, Florida, last week, everyone got on their feet when Audrey Nethery took the stage.

When is Audrey nethery birthday?

Audrey Nethery was born on October 20, 2008, in Kentucky, US.

Who discovered Diamond-Blackfan anemia?

First described in 1938 by Boston Children’s Hospital doctors Kenneth Blackfan, MD, and Louis Diamond, MD (who later established Dana-Farber/Boston Children’s Cancer and Blood Disorders Center), DBA is a potentially life-threatening condition that can cause severe anemia and other abnormalities.

Who is most likely to get Diamond-Blackfan anemia?

Diamond-Blackfan anemia, also known as acquired pure red cell aplasia, is usually diagnosed when a child is less than a year old. It’s caused by changes, or mutations, in their genes, which are the building blocks of DNA. Sometimes the genetic mutation is passed down from one parent to a child.

What is Audrey’s condition?

But for Audrey Nethery, a YouTube dancing sensation, such videos have offered a global platform to raise awareness of a rare inherited bone marrow syndrome. Nethery was born with this disease, known as Diamond-Blackfan anemia.

How old is Audrey Nethery from YouTube?

Audrey Nethery was born on October 20, 2008, in Kentucky, US. Her parents, Scott and Julie, are her support system.

How old is Audrey Nethery from Youtube?

What is Diamond Blackfan anemia (DBA)?

Diamond Blackfan anemia (DBA) is a rare blood disorder that affects the bone marrow. The function of the bone marrow is to make new blood cells, including red blood cells (which carry oxygen to the body’s tissues), white blood cells (which help the body fight infections), and platelets (which help the body stop bleeding).

What are the survival rates of Diamond Blackfan anemia?

What are the survival rates of Diamond Blackfan anemia? Children with DBA can live long lives with treatments. Some people treated for DBA achieve complete remission and do not need treatment, meaning their symptoms go away for more than six months. This can last for years and can become permanent.

What are the complications of Diamond-Blackfan anemia?

People with Diamond-Blackfan anemia have an increased risk of several serious complications related to their malfunctioning bone marrow. Specifically, they have a higher-than-average chance of developing myelodysplastic syndrome (MDS), which is a disorder in which immature blood cells fail to develop normally.

What is the hematological phenotype of Diamond-Blackfan anemia?

Diamond-Blackfan anemia (DBA) is manifested by a wide variety of clinical and in vitro abnormalities. Despite this biological diversity, the hematological phenotype is remarkably similar for all patients and consists of a normochromic-macrocytic anemia in early childhood, reticulocytopenia, and a no …