Cerebral Creatine Deficiency Syndromes

• Autor(a) principal: Malheiro, Rui
• Data de Publicação: 2013
• Outros Autores: Diogo, Luísa, Garcia, Paula, Fineza, Isabel, Oliveira, Guiomar
• Tipo de documento: Artigo
• Idioma: por
• Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
• Texto Completo: https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/1355

Introduction: Creatine deficiency syndromes are a recently described group of diseases characterized by inborn errors of creatinemetabolism. Clinical features include a spectrum of neurodevelopment disorders of diverse severity. They are characterized by lowlevels of cerebral creatine caused by different pathogenic mutations concerning the genes coding for creatine synthesis enzymes[arginine: glicyne amidinotransferase (AGAT, EC 2.1.4.1) and guanidinoacetate methyltansferase (GAMT, EC 2.1.1.2)], AGAT andGAMT, respectively, or its transporter (CT1 deficiency), SLC6A8. Enzymatic deficiencies are transmitted as autosomal recessive traits,whereas the transporter deficit is X-linked.Objectives: To characterize the clinical and laboratorial presentation, diagnosis and treatment of cerebral creatine deficiency patients,followed in Hospital Pediátrico Carmona da Mota. The awareness of these inborn errors of metabolism as neurological disorders,namely of neurodevelopment, among the medical community is a secondary aim of the present work.Methods and Material: Retrospective analysis of the clinical files of patients followed in our Hospital and diagnosed with cerebralcreatine deficiency syndrome.Results: Twelve patients belonging to seven different families were diagnosed with creatine deficiency syndromes. Five presentedGAMT deficiency and seven CT1 deficiency. Present ages are 2 to 38 years old. The most common clinical presentations were: globaldevelopment delay in seven patients (two with epilepsy), and speech delay in two patients. Only one patient had communication andsocial interaction dysfunction. In all, global development delay in the range of intellectual delay was identified. The pathognomonic patternof cerebral creatine deficiency in the brain image was demonstrated in eight patients. Pathogenic mutations in GAMT or SLC6A8genes were identified in all cases.Conclusions: The suspicion of cerebral creatine depletion must be considered in all children presenting unexplained global psychomotordevelopment delay. Pre-symptomatic therapy has shown promising results, especially in GAMT deficiency patients. The high rate ofasymptomatic carriers of GAMT mutations in our population makes this disorder eligible to neonatal screening in Portugal.