麻豆果冻传媒

Platelet disorders

Platelet disorders can include immune thrombocytopenia (ITP), a condition in which the blood doesn't clot normally because of a low number of platelets, or other inherited platelet disorders such as thrombocytopathies.

Hemophilia聽and other inherited bleeding disorders

Hemophilia聽is caused by an inherited deficiency of clotting factor proteins, which results in lifelong bleeding risk.

翱耻谤听expert care team聽has been treating patients with hemophilia and other bleeding disorders for more than 40 years. We are a lifelong partner to your child with hemophilia. As a comprehensive, federally funded hemophilia treatment center, we provide care from infancy through adulthood.

We provide the latest treatment options, including clinical trials studying gene therapy. We also strive to improve quality of life and address all aspects of the disease through services such as genetic counseling, family planning and聽physical therapy.

Iron-deficiency anemia

Iron-deficiency anemia is a very common condition in which the blood doesn鈥檛 have high enough levels of iron to produce enough hemoglobin to carry oxygen throughout the body. As a result, people with iron-deficiency anemia may be tired and short of breath. Iron deficiency anemia can usually be corrected by taking iron supplements, but additional tests or treatments may be necessary.

Thalassemia

Thalassemia聽is an inherited disorder that affects hemoglobin, a protein in red blood cells that carries oxygen. We care for one of the largest groups of thalassemia patients in the country, and we develop comprehensive treatment plans for your child鈥檚 unique needs.

Sickle cell disease

Sickle cell disease聽is an inherited disorder in which hemoglobin, a protein in red blood cells that carries oxygen, becomes stiff, sticky, and sickle shaped. These sickle cells tend to cluster together and cannot easily move through the blood vessels, causing a blockage. Our care team is experienced in using proven聽treatments聽to give our patients the best possible chance at living long, healthy lives, and we are also pioneering new treatments such as gene editing.

Hemolytic anemia

Children with hereditary聽hemolytic anemia聽have red blood cells with weakened outer membranes that burst easily, causing the blood cells to die faster than they can be replaced. If your child with hereditary hemolytic anemia needs a liver transplant, he or she will be in the best hands at 麻豆果冻传媒 Children鈥檚 Health and Lucile Packard Children鈥檚 Hospital Stanford. 翱耻谤听Pediatric Transplant Center聽has performed more聽pediatric liver transplants聽than any other U.S. hospital in the past five years, and our three-year liver patient outcomes are the best in the nation.

Red cell aplasia

Red cell aplasia is a rare condition in which the bone marrow doesn鈥檛 produce enough red blood cells, which can make patients feel tired or lead to pale skin.聽

Children with聽aplastic anemia聽don鈥檛 produce enough red and white blood cells and platelets. Aplastic anemia can either be acquired as an autoimmune disease with no known cause, or it can be inherited via genes passed from parent to child.

We care for the largest number of aplastic anemia patients at any children鈥檚 hospital in the United States, and we will work with your family to develop the best treatment plan for your child. We work closely with the聽Pediatric Stem Cell Transplantation team聽to ensure that any patient who needs a stem cell transplant will have a seamless experience. We are a founding member of the聽North American Pediatric Aplastic Anemia Consortium, a group of doctors and researchers that comes together to improve care and identify new treatments for aplastic anemia.

Langerhans cell histiocytosis (LCH)聽results from uncontrolled growth in the number of histiocyte cells, which are white blood cells in the body鈥檚 tissues. When these cells start to build up in bones, skin, and other organs, they can cause pain, swelling, and damage.

Our LCH care team includes experts in blood diseases and聽endocrinology聽because diabetes is often associated with LCH. The team works closely together to identify the best available treatment, which may include chemotherapy, radiation therapy, or surgery, while maintaining your child鈥檚 quality of life. Our program has a unique clinic that brings together doctors from many specialties to help treat the lasting effects of LCH in adolescent and adult patients.

Our team also has deep expertise caring for patients with other rare histiocytoses, including:

• Hemophagocytic lymphohistiocytosis.
• Rosai鈥揇orfman disease.
• Erdheim鈥揅hester disease.
• Juvenile xanthogranuloma.

The vascular system is the body鈥檚 plumbing, and it is made up of four types of 鈥減ipes鈥� called vessels, which carry different body fluids. Arteries carry blood away from the heart, veins carry blood back to the heart, capillaries are tiny vessels that deliver oxygen to tissues, and lymphatic vessels carry lymphatic fluid through the body. Vascular malformations are abnormally formed blood vessels, and聽vascular anomalies聽occur when blood vessels grow without control. This may lead to pain and increased clotting and bleeding risks.

Our听迟别补尘聽will work with you to develop the best treatment plan for your child. In addition to pediatric hematologists, the team includes:

• Pediatric dermatologists.
• Otolaryngologists.
• Plastic surgeons.
• Radiologists.
• Interventional radiologists.
• General surgeons.

We treat a wide range of conditions, including:

• Arteriovenous malformation (AVM).
• Capillary malformation.
• Infantile hemangioma.
• Lymphatic malformation.
• Venous malformation.
• Other vascular anomalies.

Children with聽Diamond-Blackfan anemia聽don鈥檛 produce enough red blood cells in their bone marrow, which can result in fatigue, weakness, and pale skin.

翱耻谤听care team聽includes internationally recognized experts in Diamond-Blackfan anemia care and research, including聽Kathleen Sakamoto, MD, PhD, and our doctors and scientists are working on聽聽for this rare disease.