RENATAL DIAGNOSIS IN MITOCHONDRIAL DISEASES -CASE REPORT

Autor: Andreea Serban, Laurentiu Camil Bohiltea, Cristian Strungaru, Ruxandra Cretu, Daniela Neagos

Publikováno v: Analele Ştiinţifice Ale Universităţii Alexandru Ioan Cuza din Iași,Sectiunea II A : Genetica si Biologie Moleculara, Vol 15, Iss 2, Pp 41-44 (2016)

Lactic acidosis, hypertrophic cardiomyopathy, muscle weakness and central nervous system impairment could rise suspicion of a mitochondrial disease. Its clinical complexity makes diagnostic process often difficult. While the gravity can range from mi

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http://www.gbm.bio.uaic.ro/index.php/gbm/article/view/1115