Martínez-Frías, María LuisaMendioroz, JLópez Grondona, FermínBermejo-Sanchez, EvaRodríguez-Pinilla, ElviraAparicio, PBlanco, MCuevas Catalina, María LourdesFoguet, A.López, JAPlaja, PPantoja, ARodriguez, LauraRodríguez, AValdivia, LVázquez MS2022-02-172022-02-172003-10Boletín del ECEMC: Rev Dismor Epidemiol 2003; V (nº 2): 30-330210-3893http://hdl.handle.net/20.500.12105/13661Dismorfología, Citogenética y Clínica: Resultados sobre los datos del ECEMCThis section is based on two facts: First, that the majority of the malformation syndromes are very few frequent. Second, the progressive generalization in our country of the prenatal diagnosis with a high resolution echography performed to all women between 18-20 weeks of gestation as a Service of the National Health System, together with the possibility of voluntary interruption of gestation if fetal anomalies are detected. Thus, the impact of prenatal diagnosis is that the frequency at birth of these syndromes shows an important and progressive decreasing trend. For these reasons, in addition to the difficulty for pediatricians and geneticists or our population to diagnose these usually rare syndromes, the impact of prenatal diagnosis increases the usual difficulties that the young pediatricians and geneticists have to identify these pathologies. This increases the possibility that some affected patients can remain undiagnosed for a long time, or even never be diagnosed. As started last year in this section of the "Boletín del ECEMC", we present other six syndromes of low frequency in our country.spaVoRhttp://creativecommons.org/licenses/by-nc-sa/4.0/DismorfologíaAnomalías congénitasEpidemiologíaSíndrome de Robinow recesivoSíndrome de GoltzSíndrome de GreigSíndrome de Oto-Palato-DigitalSíndrome de KingstonSíndrome de Displasia metatropicaAtribución-NoComercial-CompartirIgual 4.0 InternacionalV230-33Boletín del ECEMC: Revista de Dismorfología y Epidemiologíaopen access