Albers Schomberg disease (osteopetrosis). Case report
DOI:
https://doi.org/10.35381/s.v.v6i1.1716Keywords:
Osteopetrosis, diagnóstico por imagen, complicaciones. (Fuente, DeCS).Abstract
Objective: To describe Albers Schomberg disease (osteopetrosis) from a case report. Methods: Descriptive observational case report. Results and Conclusions: Children are usually diagnosed immediately or shortly after birth; it is characterized by hematologic problems such as anemia, thrombocytopenia, and granulocytopenia; splenomegaly; cranial nerve compression resulting in blindness and deafness; pathologic fractures; and infections. This disease is genetically recessive and there is bone marrow failure. Despite treatment, the infantile or malignant forms remain the most severe because of anemia, hemorrhages and complicated infections, often resulting in death within the first ten years of life. In contrast, adult patients have a higher survival rate.
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