Smith-Lemli-Opitz syndrome: Bosnian and Herzegovinian experience

The aim of this paper is to present a patient with the Smith-Lemli-Opitz syndrome (SLOS), with an overview of the modality of diagnosis, and the treatment of the patient. Exome analysis showed two variants in exon 6 of the 7-dehydrocholesterol reductase ( ) gene have been determined: missense variant NM_001360.2: c.470T>C (p.Leu157Pro) and nonsense variant c.452G>A (W151*). Therefore the genotype of the patient is NM_001360.2: c.[470T>C; c.452G>A]. The proband, aged 6 years, has global developmental retardation with missing contact gaze and lacking motor development for her age and with peripheral spastic-enhanced muscle tone, and is under the supervision of children neurologists, gastroenterologists, nephrologists and cardiologists.