[Referral criteria to clinical genetics from primary care: Consensus document].
| Autor: | Ejarque Doménech I; Centro de Salud de Almácera, Valencia, Valencia, España; Consulta de Genética Clínica, Hospital Vithas Aguas Vivas, Alzira, Valencia, España. Electronic address: ejarque_ism@gva.es., Marín Reina P; Dismorfología y Asesoramiento Genético, Servicio de Neonatología, Hospital Universitari i Politècnic La Fe, Valencia, España., García-Miñaur Rica S; Instituto de Genética Médica y Molecular (INGEMM), Hospital Universitario La Paz, Madrid, España., Chirivella González I; Unidad de Consejo Genético en Cáncer, Servicio de Oncología Médica, Hospital Clínico Universitario - INCLIVA, Valencia, España., Martínez Martínez MT; Unidad de Consejo Genético en Cáncer, Servicio de Oncología Médica, Hospital Clínico Universitario - INCLIVA, Valencia, España., García Rodríguez AM; Centro de Salud Delicias I Valladolid Oeste, Valladolid, España., Álvarez de Andrés S; NIMGenetics, Madrid, España., Tellería Orriols JJ; Consulta de Genética Clínica, Hospital Clínico Universitario de Valladolid, Valladolid, España. |
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| Jazyk: | Spanish; Castilian |
| Zdroj: | Atencion primaria [Aten Primaria] 2022 Dec; Vol. 54 (12), pp. 102501. Date of Electronic Publication: 2022 Nov 11. |
| DOI: | 10.1016/j.aprim.2022.102501 |
| Abstrakt: | Introduction: Primary care (PC) is the first contact between the patient and the doctor, so it is essential to be clear about the criteria for suspecting a genetic disease and where it should be referred for study. Material and Methods: Four scientific societies: the Spanish Society of Family and Community Medicine (semFYC), the Spanish Association of Human Genetics (AEGH), the Spanish Association of Pediatrics (AEP) and the Spanish Society of Medical Oncology (SEOM), have reviewed the criteria for referral to the clinical genetics services of the different published guidelines with the purpose of define the recommendations for PC. Conclusions: With this consensus document, the PC doctor and pediatrician will know when, how and where to refer their patients with hereditary and/or genetic pathology to clinical genetics services. (Copyright © 2022 The Authors. Publicado por Elsevier España, S.L.U. All rights reserved.) |
| Databáze: | MEDLINE |
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