Gaucher disease: a case study

Gaucher disease (gd) is an autosomal recessive hereditary disorder, which causes disturbances on target organs such as liver, spleen, nervous system, bone marrow and lungs. Case report: A five-year-old male patient with persistent episodes of epistaxis with two weeks of progression, limb ecchymosis...

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Detalles Bibliográficos
Autores: Lucio García, César, Noriega-Salas, Lorena
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2017
País:México
Institución:UNIVERSIDAD NACIONAL AUTÓNOMA DE MÉXICO
Repositorio:Atención Familiar
Idioma:español
OAI Identifier:oai:ojs.pkp.sfu.ca:article/61934
Acceso en línea:https://www.revistas.unam.mx/index.php/atencion_familiar/article/view/61934
Access Level:acceso abierto
Palabra clave:enfermedad de Gaucher
enfermedades de depósitos lisosomales
desórdenes genéticos
Gaucher disease
lysosomal storage diseases
genetic disorders
Descripción
Sumario:Gaucher disease (gd) is an autosomal recessive hereditary disorder, which causes disturbances on target organs such as liver, spleen, nervous system, bone marrow and lungs. Case report: A five-year-old male patient with persistent episodes of epistaxis with two weeks of progression, limb ecchymosis and hepatosplenomegaly, pain in the limbs, progressive loss of muscle strength, psychomotor regression during 10 months, and myoclonic epilepsy. The X-ray from long bones showed the shape of an Erlenmeyer flask, bone marrow biopsy with hypercellularity, due to abundant foamy histiocytes and lysosomal accumulation. We integrated the diagnosis and stratification of eg type iii b. Conclusion: enzyme replacement therapy imiglucerase, topiramate, calcitriol and calcium carbonate improved the clinical condition of the patient.