The study of splenomegaly, and the follow-up of splenectomized patients, is one of the causes of referral of these patients to pediatric gastroenterology and oncohematology clinics, and adult internal medicine and hematology. It has been described that 0.3% of hospital admissions is for this reason. The study and management of splenomegaly is well described among the different medical specialties to which these patients arrive. After the application of the different algorithms and the different studies that are carried out, these splenomegaly are identified as being of hepatic, infectious, inflammatory, congestive, hematological origin and primary causes. Despite these studies of splenomegaly, approximately 10-15% of these patients still remain undiagnosed. The objective of the present study is to increase the diagnostic sensitivity of these unknown splenomegalys, or unknown splenomegaly patients who remain in consultations, using the usual diagnostic clinical procedures of unknown splenomegaly and unknown splenectomy patients, where the investigators include the extraction of a blood sample for dry drop test (DBS), where the determination of the enzymatic/genetic activity will be carried out for Gaucher disease (GD) and acid sphingomyelinase deficiency (ASMD) , analysis of LisoGl1 and LisoSM.
Study Type
OBSERVATIONAL
Enrollment
122
No interventional study
Hospital General Universitario de Alicante
Alicante, Alicante, Spain
Hospital de Poniente
El Ejido, Almería, Spain
Hospital Universitario de Badajoz
Badajoz, Badajoz, Spain
Hospital Vall d'Hebron
Barcelona, Barcelona, Spain
Hospital Universitario Juan Ramón Jiménez
Huelva, Huelva, Spain
Complejo Hospitalario Universitario La Coruña - CHUAC
A Coruña, La Coruña, Spain
Complejo Hospitalario Universitario de Santiago - CHUS
Santiago de Compostela, La Coruña, Spain
Hospital Universitario Lucus Augusti
Lugo, Lugo, Spain
Hospital Universitario La Princesa
Madrid, Madrid, Spain
Hospital Universitario de Cabueñes
Gijón, Principality of Asturias, Spain
...and 4 more locations
Prevalence of Gaucher disease (GD) and acid sphingomyelinase deficiency (ASMD)
Determinate the prevalence of Gaucher disease (GD) and acid sphingomyelinase deficiency (ASMD)
Time frame: 36 months
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