Dreamgenics 
In the latest issue of IM Médico magazine dedicated to the specialty of Ophthalmology, we have published an article entitled "Application of massive sequencing to the diagnosis of ophthalmologic diseases" in which our colleagues Leyre Larzabal and Carlos Martínez discuss the usefulness of this technology and the improvement it has brought in the diagnosis of ophthalmologic diseases.
World Birth Defects Day is an awareness day celebrated annually on March 3 with the aim of promoting prevention and research of these diseases. What are congenital anomalies? Congenital anomalies are disorders of the morphological, structural or functional development of an organ or system that are caused by the ... Read More
Geneticist's Day is celebrated every February 8 in honor of Gregor Johann Mendel, considered worldwide as the father of genetics. The diagnosis of genetic diseases depends to a large extent on the knowledge of the disease itself and its genetic basis. This knowledge, together with the clinical phenotype of the patient ... Read More
In the last issue of the IMMédico Magazine an article of our team of geneticists has been published on the implication of genetic studies in neonatal screening. Currently, the detection of the diseases included in neonatal screening programs is carried out by means of different analytical techniques, but, given the limitations of these techniques, it is not ... Read more
Dreamgenics and CEU San Pablo University sign a framework agreement for educational cooperation for the joint implementation of training, consulting and research activities. The CEU San Pablo University is the largest and most traditional private educational institution in Spain, founded in 1933 as a University College and, since 1993, as a private University, with a total of more than 1,000 students, ... Read more
Last Wednesday we held an informative conference in collaboration with ASEMPA, Association of Muscular Diseases of the Principality of Asturias, in which our head of Clinical Genetics, Dr. Leyre Larzabal, spoke about neuromuscular diseases and the role of genetics in their diagnosis. We share with you the complete talk and we are at your disposal ... Read more
Objetivo Diagnóstico and Dreamgenics have signed a framework agreement of institutional collaboration to promote the genetic diagnosis of rare diseases, as well as to develop research projects and training activities related to them. The majority of RDDs are chronic and degenerative diseases, which means that patients suffering from them face chronic pain, difficulties ... Read More
Today, May 17, is World Neurofibromatosis Day, a genetic disorder in which tumors form in nerve tissue, called neurofibromas, resulting in cutaneous and neurological signs, mainly affecting the quality of life of patients. Different types of neurofibromatosis There are three different types of neurofibromatosis ... Read More
Yesterday we participated in the IMMeeting organized by IMMédico to talk about rare diseases, their diagnosis and treatment, together with Beatriz Perales, member of the Spanish Association of Orphan and Ultra-Orphan Drug Laboratories (AELMHU) and Ramón García, hematologist and head of the molecular biology laboratory of the University Hospital of Salamanca. Rare diseases are ... Read more
Hearing loss is the loss of hearing, to a lesser or greater degree, which may be caused by environmental or genetic causes. It is estimated that about 80% of newly diagnosed cases of hearing loss have a hereditary basis and affect, according to WHO, 360 million people worldwide. Last Thursday, we conducted a ... Read more