Your browser doesn't support javascript.
loading
Women with Gaucher Disease.
Meijon-Ortigueira, Maria Del Mar; Solares, Isabel; Muñoz-Delgado, Cecilia; Stanescu, Sinziana; Morado, Marta; Pascual-Izquierdo, Cristina; Villalon Blanco, Lucía; Belanger Quintana, Amaya; Menéndez-Conde, Covadonga Pérez; Morales-Conejo, Montserrat; Villarrubia-Espinosa, Jesús.
Afiliación
  • Meijon-Ortigueira MDM; Department of Hematology, Hospital Universitario Ramón y Cajal-IRYCIS, 28034 Madrid, Spain.
  • Solares I; Department of Internal Medicine, Clínica Universidad de Navarra, 28027 Madrid, Spain.
  • Muñoz-Delgado C; Department of Internal Medicine, Hospital Quirónsalud Sur, 28922 Madrid, Spain.
  • Stanescu S; Pediatric Metabolic Unit, Hospital Universitario Ramón y Cajal, European Reference Center (MetabERN), 28034 Madrid, Spain.
  • Morado M; Department of Hematology, Hospital Universitario La Paz, 28046 Madrid, Spain.
  • Pascual-Izquierdo C; Department of Hematology, Hospital Universitario Gregorio Marañon, 28007 Madrid, Spain.
  • Villalon Blanco L; Department of Hematology, Hospital Universitario Fundación Alcorcón, 28922 Madrid, Spain.
  • Belanger Quintana A; Pediatric Metabolic Unit, Hospital Universitario Ramón y Cajal, European Reference Center (MetabERN), 28034 Madrid, Spain.
  • Menéndez-Conde CP; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), 28029 Madrid, Spain.
  • Morales-Conejo M; Pharmacy Department, Ramón y Cajal Hospital, IRYCIS, 28034 Madrid, Spain.
  • Villarrubia-Espinosa J; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), 28029 Madrid, Spain.
Biomedicines ; 12(3)2024 Mar 05.
Article en En | MEDLINE | ID: mdl-38540192
ABSTRACT
Gaucher disease is an inherited disorder in which there is a deficiency of the enzyme glucocerebrosidase, which leads to the accumulation of glucosylceramide. Although much scientific evidence is now available, there is still limited data on the impact on the different life stages of women with this disease. Among other alterations, a delay in menarche has been described, although it has not been related to fertility problems. Menorrhagia is relatively frequent, being related to the presence of thrombocytopenia, thrombocytopathies or coagulation disorders. On the other hand, pregnancy planning is an increasingly frequent concern. All patients should undergo genetic counseling, and it is important to monitor the appearance or worsening of organomegaly, bone and hematologic abnormalities to establish clinical and therapeutic recommendations. Management during the puerperium will depend on the evolution of gestation, and, during the lactation period, the potential appearance of bone complications should be assessed. An early onset of menopause, compared to the general population, has also been described, which may accelerate the development of osteopenia. Finally, although the usual screening protocols for neoplasms are currently being performed, it is recommended to watch for early signs of liver or renal neoplasms when examining the results of imaging tests performed during evaluations for this disease.
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Biomedicines Año: 2024 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Biomedicines Año: 2024 Tipo del documento: Article País de afiliación: España