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Aase Syndrome
Alternate Names : Aase-Smith Syndrome
Definition Aase syndrome is a rare, inherited disorder characterized by anemia with some joint and skeletal deformities.
Overview, Causes, & Risk Factors
Aase syndrome is thought to be an autosomal dominant inherited disorder. The genetic basis of the disease is not known. The anemia is caused by underdevelopment of the bone marrow, which is where blood cells are formed.
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Jump to another section
• Definition
• Aase Syndrome Overview, Causes, & Risk Factors
• Aase Syndrome Symptoms & Signs
• Aase Syndrome Prevention
• Aase Syndrome Diagnosis & Tests
• Aase Syndrome Treatment
• Aase Syndrome Prognosis
• Aase Syndrome Complications
• Calling Your Health Care Provider
Topics that might be of interest to you Diseases & Conditions
• Anemia
• Ventricular Septal Defect
Tests & Exams
• Bone Marrow Biopsy
• CBC
• Echocardiogram
• WBC Count
Surgery & Procedures
• Bone Marrow Transplant
Other Topics
• Autosomal Recessive
• Cranial Sutures
• Paleness
Review Date : 8/6/2003
Reviewed By : Douglas R. Stewart, M.D., Division of Medical Genetics, Hospital of the University of Pennsylvania, Philadelphia, PA. Review provided by VeriMed Healthcare Network.
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